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BLANCHE ALTER

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Bari J Ballew; Joseph Boland; Laurie Burdett; Neelam Giri; Kevin Jacobs; BLANCHE ALTER; Meredith Yeager; Sharon A Savage
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.
BLANCHE ALTER; Philip S Rosenberg
VACTERL-H Association and Fanconi Anemia.
Andrzej Rochowski; Todd A Alonzo; Robert B Gerbing; Beverly J Lange; Susan B Olson; BLANCHE ALTER
Patients with Fanconi anemia and AML have different cytogenetic clones than de novo cases of AML.

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2013: Bari J Ballew; Joseph Boland; Laurie Burdett; Neelam Giri; Kevin Jacobs; BLANCHE ALTER; Meredith Yeager; Sharon A Savage
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.
Human genetics 2013;132(4):473-80.
2013: BLANCHE ALTER; Philip S Rosenberg
VACTERL-H Association and Fanconi Anemia.
Molecular syndromology 2013;4(1-2):87-93.
2012: Andrzej Rochowski; Todd A Alonzo; Robert B Gerbing; Beverly J Lange; Susan B Olson; BLANCHE ALTER
Patients with Fanconi anemia and AML have different cytogenetic clones than de novo cases of AML.
Pediatric blood & cancer 2012;59(5):922-4.
2012: Sandra Rackley; J J Rasimas; BLANCHE ALTER; Neelam Giri; MARYLAND PAO; Guillermo F Seratti; Sharon A Savage
Neuropsychiatric conditions among patients with dyskeratosis congenita: a link with telomere biology?
Psychosomatics 2012;53(3):230-5.
2012: Adrianna Vlachos; Philip S Rosenberg; BLANCHE ALTER; Eva Atsidaftos; Jeffrey Lipton
Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.
Blood 2012;119(16):3815-9.
2012: Kaan Boztug; George R Buchanan; John Corns; Julie Curtin; Phil Darbyshire; jean donadieu; Marie Dorda; Rachel Fruge; Jeffrey W Innis; Setareh Mamishi; Rajen J Mody; Jayashree Motwani; Thomas Moulton; Jennie Murray; William G Newman; Nima Parvaneh; Isabelle Pellier; Paolo Pierani; Nima Rezaei; Philip S Rosenberg; Hung Chi Tran; Karl Welte; BLANCHE ALTER; Zekai Avci; Siddharth Banka; Laurence A Boxer; Christoph Klein
Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.
The Journal of pediatrics 2012;160(4):679-683.e2.
2012: BLANCHE ALTER; Gabriela M Baerlocher; Neelam Giri; Peter M Lansdorp; Philip S Rosenberg; Sharon A Savage
Telomere length is associated with disease severity and declines with age in dyskeratosis congenita.
Haematologica 2012;97(3):353-9.
2012: Xi-Lei Zeng; BLANCHE ALTER; Helen B Fleisig; Neelam Giri; Kyle R Hukezalie; Sharon A Savage; Naresh R Thumati; Judy M Y Wong
The accumulation and not the specific activity of telomerase ribonucleoprotein determines telomere maintenance deficiency in X-linked dyskeratosis congenita.
Human molecular genetics 2012;21(4):721-9.
2012: Shahinaz Gadalla; Neelam Giri; Hormuzd A Katki; BLANCHE ALTER; Fatma M Shebl; Sharon A Savage
The relationship between DNA methylation and telomere length in dyskeratosis congenita.
Aging cell 2012;11(1):24-8.
2012: Yne de Vries; Cheryl R Greenberg; Sara J Israels; Hans Joenje; Bertus Kuyt; Marieke Levitus; Nikki Lwiwski; BLANCHE ALTER; Fré Arwert; Michel Zwaan; Hanne Meijers-Heijboer
A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites.
Anemia 2012;2012():865170.
2012: Andrzej Rochowski; Beverly J Lange; Philip S Rosenberg; Todd A Alonzo; Robert B Gerbing; BLANCHE ALTER
Estimation of the prevalence of Fanconi anemia among patients with de novo acute myelogenous leukemia who have poor recovery from chemotherapy.
Leukemia research 2012;36(1):29-31.
2011: Kajal Biswas; Lawrence C Brody; Sandra Burkett; R Andrew Byrd; Ranabir Das; Sergey Kuznetsov; Stefan Meyer; Susan L North; BLANCHE ALTER; Stacey Stauffer; Shyam K Sharan
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay.
Blood 2011;118(9):2430-42.
2011: Philip S Rosenberg; Hannah Tamary; BLANCHE ALTER
How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel.
American journal of medical genetics. Part A 2011;155A(8):1877-83.
2011: Andrzej Rochowski; Chunxiang Sun; Michael Glogauer; BLANCHE ALTER
Neutrophil functions in patients with inherited bone marrow failure syndromes.
Pediatric blood & cancer 2011;57(2):306-9.
2011: Luis F Z Batista; Thomas R Cech; Athena M Cherry; Jinkuk Choi; Sharon M Crary; Neelam Giri; Ha Nam Nguyen; Matthew F Pech; Renee A Reijo Pera; Sharon A Savage; Vittorio Sebastiano; Marius Wernig; Kathleen T Xie; Arthur J Zaug; Franklin L Zhong; BLANCHE ALTER; Steven E Artandi
Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells.
Nature 2011;474(7351):399-402.
2011: Sharon A Savage; Neelam Giri; Lea Jessop; Kristen Pike; Teri Plona; Laurie Burdett; BLANCHE ALTER
Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenita.
Journal of medical genetics 2011;48(4):285-8.
2011: Neelam Giri; Charles B Huddleston; Rees Lee; BLANCHE ALTER; Albert Faro; Frances V White; Sharon A Savage
Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature review.
BMC blood disorders 2011;11():3.
2011: Franklin Zhong; Sharon A Savage; Marina Shkreli; Neelam Giri; Lea Jessop; Timothy Myers; Renee Chen; BLANCHE ALTER; Steven E Artandi
Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita.
Genes & development 2011;25(1):11-6.
2011: A C Dietz; Paul J Orchard; K Scott Baker; R H Giller; S A Savage; BLANCHE ALTER; Jakub Tolar
Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita.
Bone marrow transplantation 2011;46(1):98-104.
2010: Shahinaz M Gadalla; Richard Cawthon; Neelam Giri; BLANCHE ALTER; Sharon A Savage
Telomere length in blood, buccal cells, and fibroblasts from patients with inherited bone marrow failure syndromes.
Aging 2010;2(11):867-74.
2010: Hannah Tamary; Daniella Nishri; Joanne Yacobovich; Rama Zilber; Orly Dgany; Tatyana Krasnov; Shraga Aviner; Polina Stepensky; Shoshana Ravel-Vilk; Menachem Bitan; Chaim Kaplinsky; Ayelet Ben-Barak; Ronit Elhasid; Joseph Kapelusnik; Ariel Koren; Carina Levin; Dina Attias; Ruth Laor; Isaac Yaniv; Philip S Rosenberg; BLANCHE ALTER
Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry.
Haematologica 2010;95(8):1300-7.
2010: BLANCHE ALTER; Neelam Giri; Sharon A Savage; June A Peters; Jennifer T Loud; Lisa Leathwood; Ann G Carr; Mark H Greene; Philip S Rosenberg
Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.
British journal of haematology 2010;150(2):179-88.
2010: Philip S Rosenberg; Cornelia Zeidler; Audrey Anna Bolyard; BLANCHE ALTER; Mary Ann Bonilla; Laurence A Boxer; Yigal Dror; Sally Kinsey; Daniel C Link; Peter E Newburger; Akiko Shimamura; Karl Welte; David C Dale
Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.
British journal of haematology 2010;150(2):196-9.
2010: Akiko Shimamura; BLANCHE ALTER
Pathophysiology and management of inherited bone marrow failure syndromes.
Blood reviews 2010;24(3):101-22.
2010: Ekaterini T Tsilou; Neelam Giri; Sarah Weinstein; Christine Mueller; Sharon A Savage; BLANCHE ALTER
Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenita.
Ophthalmology 2010;117(3):615-22.
2010: BLANCHE ALTER; Susan B Olson
Wilms tumor, AML, and medulloblastoma in a child with cancer prone syndrome of total premature chromatid separation and Fanconi anemia.
Pediatric blood & cancer 2010;54(3):488; author reply 489.
2010: Luoping Zhang; Xiaojiang Tang; Nathaniel Rothman; Roel Vermeulen; Zhiying Ji; Min Shen; Chuangyi Qiu; Weihong Guo; Songwang Liu; Boris Reiss; Laura Beane Freeman; Yichen Ge; Alan E Hubbard; Ming Hua; Aaron Blair; Noe Galvan; Xiaolin Ruan; BLANCHE ALTER; Kerry X Xin; Senhua Li; Lee E Moore; Sungkyoon Kim; Yuxuan Xie; Richard B Hayes; Mariko Azuma; Michael Hauptmann; Jun Xiong; Patricia Stewart; Laiyu Li; Stephen M Rappaport; Hanlin Huang; Joseph F Fraumeni; Martyn T Smith; Qing Lan
Occupational exposure to formaldehyde, hematotoxicity, and leukemia-specific chromosome changes in cultured myeloid progenitor cells.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2010;19(1):80-8.
2009: Sharon A Savage; Inderjeet Dokal; Mary Armanios; Geraldine Aubert; Edward W Cowen; Demetrio L Domingo; Neelam Giri; Mark H Greene; Paul J Orchard; Jakub Tolar; Ekaterini Tsilou; Carter Van Waes; Judy M Y Wong; Neal S Young; BLANCHE ALTER
Dyskeratosis congenita: the first NIH clinical research workshop.
Pediatric blood & cancer 2009;53(3):520-3.
2009: BLANCHE ALTER; Neelam Giri; Sharon A Savage; Philip S Rosenberg
Cancer in dyskeratosis congenita.
Blood 2009;113(26):6549-57.
2009: Sharon A Savage; BLANCHE ALTER
Dyskeratosis congenita.
Hematology/oncology clinics of North America 2009;23(2):215-31.
2008: Mohamad Al-Rahawan; BLANCHE ALTER; Barbara J Bryant; M Tarek Elghetany
Bone marrow cell cycle markers in inherited bone marrow failure syndromes.
Leukemia research 2008;32(12):1793-9.
2008: Colleen C Denny; Benjamin S Wilfond; June A Peters; Neelam Giri; BLANCHE ALTER
All in the family: disclosure of "unwanted" information to an adolescent to benefit a relative.
American journal of medical genetics. Part A 2008;146A(21):2719-24.
2008: Adrianna Vlachos; Sarah Ball; Niklas Dahl; BLANCHE ALTER; Sujit Sheth; Ugo Ramenghi; Joerg Meerpohl; Stefan Karlsson; Johnson Ming-Yu Liu; Thierry Leblanc; Carole Paley; Elizabeth M Kang; Eva Judmann Leder; Eva Atsidaftos; Akiko Shimamura; Monica Bessler; Bertil Glader; Jeffrey Lipton
Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference.
British journal of haematology 2008;142(6):859-76.
2008: Jane C Atkinson; K E Harvey; D L Domingo; M I Trujillo; J P Guadagnini; S Gollins; N Giri; Thomas Hart; BLANCHE ALTER
Oral and dental phenotype of dyskeratosis congenita.
Oral diseases 2008;14(5):419-27.
2008: Philip S Rosenberg; BLANCHE ALTER; Wolfram Ebell
Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry.
Haematologica 2008;93(4):511-7.
2008: Sharon A Savage; Neelam Giri; Gabriela M Baerlocher; Nick Orr; Peter M Lansdorp; BLANCHE ALTER
TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita.
American journal of human genetics 2008;82(2):501-9.
2008: Sharon A Savage; BLANCHE ALTER
The role of telomere biology in bone marrow failure and other disorders.
Mechanisms of ageing and development 2008;129(1-2):35-47.
2008: Philip S Rosenberg; BLANCHE ALTER; Daniel C Link; Steven Stein; Elin Rodger; Audrey Anna Bolyard; Andrew A G Aprikyan; Mary Ann Bonilla; Yigal Dror; George Kannourakis; Peter E Newburger; Laurence A Boxer; David C Dale
Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia.
British journal of haematology 2008;140(2):210-3.
2007: Neelam Giri; Paul A Pitel; David Green; BLANCHE ALTER
Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor.
British journal of haematology 2007;138(6):815-7.
2007: BLANCHE ALTER; Gabriela M Baerlocher; Sharon A Savage; STEPHEN CHANOCK; Babette B Weksler; Judith P Willner; June A Peters; Neelam Giri; Peter M Lansdorp
Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
Blood 2007;110(5):1439-47.
2007: Neelam Giri; Dalia L Batista; BLANCHE ALTER; Constantine Straturis
Endocrine abnormalities in patients with Fanconi anemia.
The Journal of clinical endocrinology and metabolism 2007;92(7):2624-31.
2007: BLANCHE ALTER; Philip S Rosenberg
Granulocyte colony-stimulating factor and severe aplastic anemia.
Blood 2007;109(10):4589; author reply 4589-90.
2007: Hannah Tamary; BLANCHE ALTER
Current diagnosis of inherited bone marrow failure syndromes.
Pediatric hematology and oncology 2007;24(2):87-99.
2007: BLANCHE ALTER
Diagnosis, genetics, and management of inherited bone marrow failure syndromes.
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2007;():29-39.
2007: BLANCHE ALTER; Philip S Rosenberg; Lawrence C Brody
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
Journal of medical genetics 2007;44(1):1-9.
2007: Sadie Pauline Hutson; BLANCHE ALTER
Experiences of siblings of patients with Fanconi anemia.
Pediatric blood & cancer 2007;48(1):72-9.
2006: Sharon A Savage; Brian J Stewart; Babette B Weksler; Gabriela M Baerlocher; Peter M Lansdorp; STEPHEN CHANOCK; BLANCHE ALTER
Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure.
Blood cells, molecules & diseases 2006;37(2):134-6.
2006: David C Dale; Philip S Rosenberg; BLANCHE ALTER
Lineage-specific hematopoietic growth factors.
The New England journal of medicine 2006;355(5):526-7; author reply 527.
2006: David C Dale; Audrey Anna Bolyard; Beate G Schwinzer; Gusal Pracht; Mary Ann Bonilla; Laurence A Boxer; Melvin H Freedman; jean donadieu; George Kannourakis; BLANCHE ALTER; Bonnie P Cham; Jerry Winkelstein; Sally E Kinsey; Cornelia Zeidler; Karl Welte
The Severe Chronic Neutropenia International Registry: 10-Year Follow-up Report.
Supportive cancer therapy 2006;3(4):220-31.
2006: Grover C Bagby; BLANCHE ALTER
Fanconi anemia.
Seminars in hematology 2006;43(3):147-56.
2006: Philip S Rosenberg; BLANCHE ALTER; Audrey Anna Bolyard; Mary Ann Bonilla; Laurence A Boxer; Bonnie Cham; Carol J Fier; Melvin Freedman; George Kannourakis; Sally E Kinsey; Beate Schwinzer; Cornelia Zeidler; Karl Welte; David C Dale
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy.
Blood 2006;107(12):4628-35.
2006: Marisa Braun; Neelam Giri; BLANCHE ALTER; Edward W Cowen
Thrombocytopenia, multiple mucosal squamous cell carcinomas, and dyspigmentation.
Journal of the American Academy of Dermatology 2006;54(6):1056-9.
2006: BLANCHE ALTER
The association between FANCD1/BRCA2 mutations and leukaemia.
British journal of haematology 2006;133(4):446-8; author reply 448.
2006: Mohamad Al-Rahawan; Neelam Giri; BLANCHE ALTER
Intensive immunosuppression therapy for aplastic anemia associated with dyskeratosis congenita.
International journal of hematology 2006;83(3):275-6.
2006: Lois B Travis; Charles S Rabkin; Linda Morris Brown; James M Allan; BLANCHE ALTER; Christine B Ambrosone; Colin B Begg; Neil Caporaso; STEPHEN CHANOCK; Angela DeMichele; William Douglas Figg; Mary K Gospodarowicz; Eric J Hall; Michie Hisada; Peter D Inskip; Ruth A Kleinerman; John B Little; David Malkin; Andrea K Ng; Kenneth Offit; Ching-Hon Pui; Leslie L Robison; Nathaniel Rothman; Peter G Shields; Louise Strong; Toshiyasu Taniguchi; Margaret A Tucker; Mark H Greene
Cancer survivorship--genetic susceptibility and second primary cancers: research strategies and recommendations.
Journal of the National Cancer Institute 2006;98(1):15-25.
2005: BLANCHE ALTER
Fanconi's anemia, transplantation, and cancer.
Pediatric transplantation 2005;9 Suppl 7():81-6.
2005: Qing Lan; Luoping Zhang; Min Shen; Martyn T Smith; Guilan Li; Roel Vermeulen; Stephen M Rappaport; Matthew Forrest; Richard Hayes; Martha Linet; Mustafa Dosemeci; BLANCHE ALTER; Rona S Weinberg; Songnian Yin; Meredith Yeager; Robert Welch; Suramya Waidyanatha; Sungkyoon Kim; STEPHEN CHANOCK; Nathaniel Rothman
Polymorphisms in cytokine and cellular adhesion molecule genes and susceptibility to hematotoxicity among workers exposed to benzene.
Cancer research 2005;65(20):9574-81.
2005: Philip S Rosenberg; BLANCHE ALTER; Gérard Socié; Eliane Gluckman
Secular trends in outcomes for Fanconi anemia patients who receive transplants: implications for future studies.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2005;11(9):672-9.
2005: BLANCHE ALTER; Hans Joenje; Anneke B Oostra; Gerard Pals
Fanconi anemia: adult head and neck cancer and hematopoietic mosaicism.
Archives of otolaryngology--head & neck surgery 2005;131(7):635-9.
2005: BLANCHE ALTER
Bone marrow failure: a child is not just a small adult (but an adult can have a childhood disease).
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program 2005;():96-103.
2005: Philip S Rosenberg; Gérard Socié; BLANCHE ALTER; Eliane Gluckman
Risk of head and neck squamous cell cancer and death in patients with Fanconi anemia who did and did not receive transplants.
Blood 2005;105(1):67-73.
2004: Qing Lan; Luoping Zhang; Guilan Li; Roel Vermeulen; Rona S Weinberg; Mustafa Dosemeci; Stephen M Rappaport; Min Shen; BLANCHE ALTER; Yongji Wu; William Kopp; Suramya Waidyanatha; Charles S Rabkin; Weihong Guo; STEPHEN CHANOCK; Richard Hayes; Martha Linet; Sungkyoon Kim; Songnian Yin; Nathaniel Rothman; Martyn T Smith
Hematotoxicity in workers exposed to low levels of benzene.
Science (New York, N.Y.) 2004;306(5702):1774-6.
2004: Isela Velazquez; BLANCHE ALTER
Androgens and liver tumors: Fanconi's anemia and non-Fanconi's conditions.
American journal of hematology 2004;77(3):257-67.
2004: BLANCHE ALTER
Growth hormone and the risk of malignancy.
Pediatric blood & cancer 2004;43(5):534-5.
2004: Philip S Rosenberg; Yi Huang; BLANCHE ALTER
Individualized risks of first adverse events in patients with Fanconi anemia.
Blood 2004;104(2):350-5.
2004: Betty C Tong; Karan Dhir; Patrick K Ha; William H Westra; BLANCHE ALTER; David Sidransky; Wayne M Koch; Joseph A Califano
Use of single nucleotide polymorphism arrays to identify a novel region of loss on chromosome 6q in squamous cell carcinomas of the oral cavity.
Head & neck 2004;26(4):345-52.
2003: BLANCHE ALTER; M Tarek Elghetany
The CCC system: is it really the answer to pediatric MDS?
Journal of pediatric hematology/oncology 2003;25(5):426-7; author reply 427-8.
2003: BLANCHE ALTER; Mark H Greene; Isela Velazquez; Philip S Rosenberg
Cancer in Fanconi anemia.
Blood 2003;101(5):2072.
2003: Philip S Rosenberg; Mark H Greene; BLANCHE ALTER
Cancer incidence in persons with Fanconi anemia.
Blood 2003;101(3):822-6.
2003: BLANCHE ALTER
Cancer in Fanconi anemia, 1927-2001.
Cancer 2003;97(2):425-40.
2002: Melvin H Freedman; BLANCHE ALTER
Malignant myeloid transformation in congenital forms of neutropenia.
The Israel Medical Association journal : IMAJ 2002;4(11):1011-4.
2002: BLANCHE ALTER
Bone marrow failure syndromes in children.
Pediatric clinics of North America 2002;49(5):973-88.
2002: Robert Rothbaum; Jean Perrault; Adrianna Vlachos; Marco Cipolli; BLANCHE ALTER; Susan Burroughs; Peter Roy Durie; M Tarek Elghetany; Richard Grand; Van Hubbard; Johanna Rommens; Thomas Rossi
Shwachman-Diamond syndrome: report from an international conference.
The Journal of pediatrics 2002;141(2):266-70.
2002: Melvin H Freedman; BLANCHE ALTER
Risk of myelodysplastic syndrome and acute myeloid leukemia in congenital neutropenias.
Seminars in hematology 2002;39(2):128-33.
2002: M Tarek Elghetany; BLANCHE ALTER
p53 protein overexpression in bone marrow biopsies of patients with Shwachman-Diamond syndrome has a prevalence similar to that of patients with refractory anemia.
Archives of pathology & laboratory medicine 2002;126(4):452-5.
2002: BLANCHE ALTER
Radiosensitivity in Fanconi's anemia patients.
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology 2002;62(3):345-7.
2001: M Kumar; Kwesi Sackey; Frank C Schmalstieg; Z Trizna; M Tarek Elghetany; BLANCHE ALTER
Griscelli syndrome: rare neonatal syndrome of recurrent hemophagocytosis.
Journal of pediatric hematology/oncology 2001;23(7):464-8.
2001: BLANCHE ALTER
Modern review of congenital hypoplastic anemia.
Journal of pediatric hematology/oncology 2001;23(6):383-4.
2001: Jonathan Flint; Cristina Tufarelli; JF Peden; Kevin Clark; Rachael J Daniels; Ross Hardison; Webb Miller; Sjaak Philipsen; Kian-Cheng Tan-Un; Tara McMorrow; Jon Frampton; BLANCHE ALTER; Anna-Maria Frischauf; Douglas R Higgs
Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster.
Human molecular genetics 2001;10(4):371-82.
2000: Elizabeth M Petty; Gregory Yanik; Raymond J Hutchinson; BLANCHE ALTER; Frank C Schmalstieg; John E Levine; David Ginsburg; J E Robillard; Valerie P Castle
Successful bone marrow transplantation in a patient with Schimke immuno-osseous dysplasia.
The Journal of pediatrics 2000;137(6):882-6.
2000: BLANCHE ALTER; J P Caruso; R A Drachtman; T Uchida; Gopalrao Velagaleti; M Tarek Elghetany
Fanconi anemia: myelodysplasia as a predictor of outcome.
Cancer genetics and cytogenetics 2000;117(2):125-31.
2000: BLANCHE ALTER
Molecular medicine and bone marrow failure syndromes.
The Journal of pediatrics 2000;136(3):275-6.
1999: BLANCHE ALTER; M Kumar; L L Lockhart; P G Sprinz; Thomas F Rowe
Pregnancy in bone marrow failure syndromes: Diamond-Blackfan anaemia and Shwachman-Diamond syndrome.
British journal of haematology 1999;107(1):49-54.
1999: H Y Luo; X L Liang; C Frye; M Wonio; G D Hankins; D H Chui; BLANCHE ALTER
Embryonic hemoglobins are expressed in definitive cells.
Blood 1999;94(1):359-61.
1999: BLANCHE ALTER
Bone marrow failure syndromes.
Clinics in laboratory medicine 1999;19(1):113-33.
1998: BLANCHE ALTER; R A Drachtman
Dyskeratosis congenita: nails and hands.
American journal of hematology 1998;58(4):298.
1998: J Li; Maria W Plonczynski; Martin H Steinberg; A Kheradpour; BLANCHE ALTER
Severe Hb S-beta+ thalassemia caused by IVS-I splice site mutations.
Hemoglobin 1998;22(4):383-6.
1998: M Kumar; BLANCHE ALTER
Hematopoietic growth factors for the treatment of aplastic anemia.
Current opinion in hematology 1998;5(3):226-34.
1998: BLANCHE ALTER
Bone marrow transplant in Diamond-Blackfan anemia.
Bone marrow transplantation 1998;21(9):965-6.
1998: BLANCHE ALTER
Modulation of macrocytosis in aplastic anemia.
American journal of hematology 1998;57(1):92.
1997: Y al-Awami; David A Sears; George Carrum; Mark M Udden; BLANCHE ALTER; C L Conlon
Pure red cell aplasia associated with hepatitis C infection.
The American journal of the medical sciences 1997;314(2):113-7.
1997: BLANCHE ALTER
Arms and the man or hands and the child: congenital anomalies and hematologic syndromes.
Journal of pediatric hematology/oncology 1997;19(4):287-91.
1997: BLANCHE ALTER; F H Gardner; R E Hall
Treatment of dyskeratosis congenita with granulocyte colony-stimulating factor and erythropoietin.
British journal of haematology 1997;97(2):309-11.
1997: O K Mupanomunda; BLANCHE ALTER
Transient erythroblastopenia of childhood (TEC) presenting as leukoerythroblastic anemia.
Journal of pediatric hematology/oncology 1997;19(2):165-7.
1997: M H Qazilbash; Johnson Ming-Yu Liu; Adrianna Vlachos; Steven Fruchtman; H Messner; A Zipursky; BLANCHE ALTER; Neal S Young
A new syndrome of familial aplastic anemia and chronic liver disease.
Acta haematologica 1997;97(3):164-7.
1996: BLANCHE ALTER
Fanconi's anemia and malignancies.
American journal of hematology 1996;53(2):99-110.
1996: Q Z Zhao; X L Liang; S Mitra; G Gourdon; BLANCHE ALTER
Cloning and characterization of the mouse alpha globin cluster and a new hypervariable marker.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(10):749-53.
1996: W R Rackoff; Attilio Orazi; C A Robinson; Ryan J Cooper; BLANCHE ALTER; M H Freedman; R E Harris; David A Williams
Prolonged administration of granulocyte colony-stimulating factor (filgrastim) to patients with Fanconi anemia: a pilot study.
Blood 1996;88(5):1588-93.
1995: K Ono; BLANCHE ALTER
Effects of low oxygen tension and antioxidants on human erythropoiesis in vitro.
Experimental hematology 1995;23(13):1372-7.
1995: Rona S Weinberg; R Acosta; M E Knobloch; M Garber; BLANCHE ALTER
Low oxygen enhances sickle and normal erythropoiesis and fetal hemoglobin synthesis in vitro.
Hemoglobin 1995;19(5):263-75.
1995: BLANCHE ALTER
Hematologic abnormalities in Fanconi anemia.
Blood 1995;85(4):1148-9.
1995: Richard A Drachtman; BLANCHE ALTER
Dyskeratosis congenita.
Dermatologic clinics 1995;13(1):33-9.
1994: John S Waye; Barry Eng; M B Coleman; Martin H Steinberg; BLANCHE ALTER
Delta beta-thalassemia in an African-American: identification of the deletion endpoints and PCR-based diagnosis.
Hemoglobin 1994;18(6):389-99.
1994: BLANCHE ALTER
Biology of erythropoiesis.
Annals of the New York Academy of Sciences 1994;731():36-47.
1994: BLANCHE ALTER; M S Tenner
Brain tumors in patients with Fanconi's anemia.
Archives of pediatrics & adolescent medicine 1994;148(6):661-3.
1993: BLANCHE ALTER
Diamond-Blackfan anaemia.
The Veterinary record 1993;133(22):556.
1993: BLANCHE ALTER; Angela Scalise; J McCombs; Vesna Najfeld
Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?
British journal of haematology 1993;85(3):627-30.
1993: BLANCHE ALTER
Fanconi's anaemia and its variability.
British journal of haematology 1993;85(1):9-14.
1993: AP Gillio; L B Faulkner; BLANCHE ALTER; L Reilly; R Klafter; Glenn Heller; D C Young; Jeffrey Lipton; Malcolm A S Moore; Richard J O'Reilly
Treatment of Diamond-Blackfan anemia with recombinant human interleukin-3.
Blood 1993;82(3):744-51.
1993: AP Gillio; L B Faulkner; BLANCHE ALTER; L Reilly; R Klafter; Glenn Heller; D C Young; Jeffrey Lipton; Malcolm A S Moore; Richard J O'Reilly
Successful treatment of Diamond-Blackfan anemia with interleukin 3.
Stem cells (Dayton, Ohio) 1993;11 Suppl 2():123-30.
1993: Rona S Weinberg; J C Thomson; R Lao; G Chen; BLANCHE ALTER
Stem cell factor amplifies newborn and sickle erythropoiesis in liquid cultures.
Blood 1993;81(10):2591-9.
1993: BLANCHE ALTER; T Gaston; Jeffrey Lipton
Lack of effect of corticosteroids in W/Wv and S1/S1d mice: these strains are not a model for steroid-responsive Diamond-Blackfan anemia.
European journal of haematology 1993;50(5):275-8.
1993: L R Silverman; J F Holland; R S Weinberg; BLANCHE ALTER; R B Davis; R R Ellison; E P Demakos; C J Cornell; R W Carey; Charles Alan Schiffer
Effects of treatment with 5-azacytidine on the in vivo and in vitro hematopoiesis in patients with myelodysplastic syndromes.
Leukemia 1993;7 Suppl 1():21-9.
1993: BLANCHE ALTER
Hydrocephalus in Fanconi anemia.
American journal of medical genetics 1993;45(6):785.
1992: BLANCHE ALTER; M E Knobloch; L He; A P Gillio; Richard J O'Reilly; L K Reilly; Rona S Weinberg
Effect of stem cell factor on in vitro erythropoiesis in patients with bone marrow failure syndromes.
Blood 1992;80(12):3000-8.
1992: Richard A Drachtman; BLANCHE ALTER
Dyskeratosis congenita: clinical and genetic heterogeneity. Report of a new case and review of the literature.
The American journal of pediatric hematology/oncology 1992;14(4):297-304.
1992: BLANCHE ALTER
Arm anomalies and bone marrow failure may go hand in hand.
The Journal of hand surgery 1992;17(3):566-71.
1992: BLANCHE ALTER
Fanconi's anemia. Current concepts.
The American journal of pediatric hematology/oncology 1992;14(2):170-6.
1992: Richard A Drachtman; E N Geissler; BLANCHE ALTER
The SCF and c-kit genes in Diamond-Blackfan anemia.
Blood 1992;79(8):2177-8.
1992: BLANCHE ALTER
Leukemia and preleukemia in Fanconi's anemia.
Cancer genetics and cytogenetics 1992;58(2):206-8; discussion 209.
1992: Rona S Weinberg; L Y He; BLANCHE ALTER
Erythropoiesis is distinct at each stage of ontogeny.
Pediatric research 1992;31(2):170-5.
1992: BLANCHE ALTER
Fanconi anemia in blacks.
American journal of medical genetics 1992;42(3):393-4.
1992: BLANCHE ALTER; L He; R Acosta; M E Knobloch; J C Thomson; Patricia J Giardina; Rona S Weinberg
Sickle and thalassemic erythroid progenitor cells are different from normal.
Hemoglobin 1992;16(6):447-67.
1991: Richard A Drachtman; E N Geissler; BLANCHE ALTER
TaqI RFLP at the c-kit oncogene locus (KIT).
Nucleic acids research 1991;19(24):6975.
1991: BLANCHE ALTER
Bone marrow failure disorders.
The Mount Sinai journal of medicine, New York 1991;58(6):521-34.
1991: BLANCHE ALTER; M E Knobloch; Rona S Weinberg
Erythropoiesis in Fanconi's anemia.
Blood 1991;78(3):602-8.
1991: BLANCHE ALTER; C L Frissora; D S Halpérin; M H Freedman; U Chitkara; E Alvarez; L Lynch; B Adler-Brecher; Arleen D Auerbach
Fanconi's anaemia and pregnancy.
British journal of haematology 1991;77(3):410-8.
1990: Rona S Weinberg; D Leibowitz; M E Weinblatt; J Kochen; BLANCHE ALTER
Juvenile chronic myelogenous leukaemia: the only example of truly fetal (not fetal-like) erythropoiesis.
British journal of haematology 1990;76(2):307-10.
1990: T Coetzer; J Palek; J Lawler; Shih-Chun Liu; Petr Jarolim; M Lahav; Josef T Prchal; W Wang; BLANCHE ALTER; G Schewitz
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
Blood 1990;75(11):2235-44.
1990: BLANCHE ALTER
Agranulocytosis and thrombocytopenia, Blackfan-Diamond anaemia, and oral chelation.
Lancet 1990;335(8695):970.
1990: BLANCHE ALTER
Antenatal diagnosis. Summary of results.
Annals of the New York Academy of Sciences 1990;612():237-50.
1989: M. Catherine Driscoll; Carl Dobkin; BLANCHE ALTER
Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(19):7470-4.
1989: Rona S Weinberg; A Worsley; H S Gilbert; J Cuttner; P D Berk; BLANCHE ALTER
Comparison of erythroid progenitor cell growth in vitro in polycythemia vera and chronic myelogenous leukemia: only polycythemia vera has endogenous colonies.
Leukemia research 1989;13(4):331-8.
1989: BLANCHE ALTER; C K Wagner; L S Susser; Rona S Weinberg
Modulation of mouse hemoglobin expression by hydroxyurea and erythropoietin in vivo.
Progress in clinical and biological research 1989;316B():317-25.
1989: BLANCHE ALTER; J M Schofield; L Y He; Rona S Weinberg
Effects of hemin on erythropoiesis.
Advances in experimental medicine and biology 1989;271():95-102.
1989: BLANCHE ALTER; M A Weiner; M B Harris
Erythrocyte characteristics in childhood acute leukemia.
The American journal of pediatric hematology/oncology 1989;11(1):8-15.
1988: S Ganguly; Arthur I Skoultchi; Michael D Garrick; Laura M Garrick; A S Campbell; BLANCHE ALTER
Differential synthesis of beta-major and beta-minor globin proteins in murine erythroleukemia cells is regulated at the transcriptional level.
The Journal of biological chemistry 1988;263(7):3216-9.
1988: BLANCHE ALTER; Rona S Weinberg; Joel A Brochstein; Richard J O'Reilly
Erythropoiesis following bone marrow transplantation for thalassemia major.
Birth defects original article series 1988;23(5B):317-21.
1988: BLANCHE ALTER; J D Goldberg; R L Berkowitz
Red cell size heterogeneity during ontogeny.
The American journal of pediatric hematology/oncology 1988;10(4):279-82.
1988: BLANCHE ALTER
Prenatal diagnosis: general introduction, methodology, and review.
Hemoglobin 1988;12(5-6):763-72.
1988: BLANCHE ALTER
Hemoglobin F switching.
Birth defects original article series 1988;23(5B):331-7.
1987: M D Garrick; R A Popp; BLANCHE ALTER
Primary structure of two nonallelic beta-globin chains from DBA/2 mice.
Biochemical genetics 1987;25(5-6):391-9.
1987: BLANCHE ALTER; DD Stump
Prenatal diagnosis of hemoglobinopathies: a potential application of high performance liquid chromatography.
Hemoglobin 1987;11(4):341-52.
1987: F J Kaye; Rona S Weinberg; J M Schofield; BLANCHE ALTER
The effect of hemin in vitro and in vivo on human erythroid progenitor cells.
International journal of cell cloning 1987;5(1):74-88.
1987: BLANCHE ALTER; C K Wagner
A murine model for hemoglobin regulation: hydroxyurea increases mouse minor hemoglobin in vivo.
Progress in clinical and biological research 1987;251():479-85.
1987: BLANCHE ALTER
Prenatal diagnosis of hematologic diseases, 1986 update.
Acta haematologica 1987;78(2-3):137-41.
1986: BLANCHE ALTER; Rona S Weinberg; D C Linch; J M Schofield; Benjamin T Jackson; GJ Piasecki; J C Thornton; D G Nathan
Investigations of the simian ontogenic switch from fetal to adult hemoglobin at the progenitor cell level.
The Journal of clinical investigation 1986;78(6):1497-503.
1986: Joel A Brochstein; D Kirkpatrick; Patricia J Giardina; Rona S Weinberg; BLANCHE ALTER; M. Catherine Driscoll; L Wolfe; B Shank; Richard J O'Reilly
Bone marrow transplantation in two multiply transfused patients with thalassaemia major.
British journal of haematology 1986;63(3):445-56.
1986: Rona S Weinberg; J M Schofield; A L Lenes; Joel A Brochstein; BLANCHE ALTER
Adult 'fetal-like' erythropoiesis characterizes recovery from bone marrow transplantation.
British journal of haematology 1986;63(3):415-24.
1985: BLANCHE ALTER; H S Gilbert
The effect of hydroxyurea on hemoglobin F in patients with myeloproliferative syndromes.
Blood 1985;66(2):373-9.
1985: BLANCHE ALTER; A Auerbach
Fanconi's anemia variant.
Blood 1985;65(5):1292.
1985: F J Kaye; BLANCHE ALTER
Red-cell size distribution analysis: an evaluation of microcytic anemia in chronically ill patients.
The Mount Sinai journal of medicine, New York 1985;52(5):319-23.
1985: BLANCHE ALTER
Neonatal pancytopenia after maternal azathioprine therapy.
The Journal of pediatrics 1985;106(4):691.
1985: BLANCHE ALTER
Antenatal diagnosis of thalassemia: a review.
Annals of the New York Academy of Sciences 1985;445():393-407.
1985: BLANCHE ALTER; H S Gilbert
Hydroxyurea and hemoglobin F in patients with myeloproliferative syndromes.
Progress in clinical and biological research 1985;191():455-61.
1984: BLANCHE ALTER; A S Campbell
Increased synthesis of mouse minor hemoglobin in erythroid colonies: a cellular model for hemoglobin regulation.
Experimental hematology 1984;12(8):611-6.
1984: BLANCHE ALTER
Advances in the prenatal diagnosis of hematologic diseases.
Blood 1984;64(2):329-40.
1984: Rona S Weinberg; S E Antonarakis; Haig Kazazian ; George J Dover; Stuart H Orkin; A L Lenes; J M Schofield; BLANCHE ALTER
Fetal hemoglobin synthesis in erythroid cultures in hereditary persistence of fetal hemoglobin and beta o-thalassemia.
Blood 1984;63(6):1278-84.
1984: C W Miller; K Young; D Dumenil; BLANCHE ALTER; J M Schofield; A Bank
Specific globin mRNAs in human erythroleukemia (K562) cells.
Blood 1984;63(1):195-200.
1983: Rona S Weinberg; J D Goldberg; J M Schofield; A L Lenes; R Styczynski; BLANCHE ALTER
Switch from fetal to adult hemoglobin is associated with a change in progenitor cell population.
The Journal of clinical investigation 1983;71(4):785-94.
1983: BLANCHE ALTER
Prenatal diagnosis of hemoglobinopathies: development of methods for study of fetal red cells and fibroblasts.
The American journal of pediatric hematology/oncology 1983;5(4):378-85.
1983: BLANCHE ALTER; Rona S Weinberg; J D Goldberg; Benjamin T Jackson; GJ Piasecki; Jeffrey Lipton; D G Nathan
Evidence for a clonal model for hemoglobin switching.
Progress in clinical and biological research 1983;134():431-42.
1982: BLANCHE ALTER; A S Campbell; J G Holland; C Friend
Increased mouse minor hemoglobin during erythroid stress: a model for hemoglobin regulation.
Experimental hematology 1982;10(9):754-60.
1982: BLANCHE ALTER; A S Campbell
New murine globin bands on electrophoresis may not be new globin chains.
Hemoglobin 1982;6(5):517-22.
1982: BLANCHE ALTER
Prenatal diagnosis of hemoglobinopathies: worldwide experience.
Birth defects original article series 1982;18(7):263-74.
1982: BLANCHE ALTER; D G Nathan
A cellular model for hemoglobin switching.
Birth defects original article series 1982;18(7):111-6.
1981: BLANCHE ALTER
Prenatal diagnosis of haemoglobinopathies: A status report.
Lancet 1981;2(8256):1152-5.
1981: G R Buchanan; BLANCHE ALTER; C A Holtkamp; E G Walsh
Platelet number and function in Diamond-Blackfan anemia.
Pediatrics 1981;68(2):238-41.
1981: M P Link; BLANCHE ALTER
Fetal-like erythropoiesis during recovery from transient erythroblastopenia of childhood (TEC).
Pediatric research 1981;15(7):1036-9.
1981: BLANCHE ALTER; Benjamin T Jackson; Jeffrey Lipton; GJ Piasecki; P L Jackson; M Kudisch; D G Nathan
Control of the simian fetal hemoglobin switch at the progenitor cell level.
The Journal of clinical investigation 1981;67(2):458-66.
1981: BLANCHE ALTER
Gel electrophoretic separation of globin chains.
Progress in clinical and biological research 1981;60():157-75.
1981: BLANCHE ALTER; E Coupal; B G Forget
Globin chain electrophoresis for prenatal diagnosis of beta thalassemia.
Hemoglobin 1981;5(4):357-70.
1981: BLANCHE ALTER; S C Goff; T J Klonowski; M D Garrik
Chemical evidence for the separation of G gamma and A gamma globin chains by polyacrylamide gel electrophoresis in urea and Triton X-100.
Preparative biochemistry 1981;11(2):217-28.
1981: BLANCHE ALTER
Pre- and postnatal diagnosis of the hemoglobinopathies.
Birth defects original article series 1981;17(1):181-99.
1980: BLANCHE ALTER; S C Goff
A murine model for the switch from fetal to adult hemoglobin during ontogeny.
Blood 1980;56(6):1100-5.
1980: BLANCHE ALTER
Intrauterine diagnosis of hemoglobinopathies.
Seminars in perinatology 1980;4(3):189-98.
1980: BLANCHE ALTER; S C Goff
Electrophoretic separation of human embryonic globin demonstrates "alpha-thalassemia" in human leukemia cell line K562.
Biochemical and biophysical research communications 1980;94(3):843-8.
1980: BLANCHE ALTER; S C Goff; Georgi D Efremov; M E Gravely; TH Huisman
Globin chain electrophoresis: a new approach to the determination of the G gamma/A gamma ratio in fetal haemoglobin and to studies of globin synthesis.
British journal of haematology 1980;44(4):527-34.
1980: BLANCHE ALTER; S C Goff
Hemoglobin switching: a cellular model.
Science (New York, N.Y.) 1980;207(4431):647-9.
1980: BLANCHE ALTER; Stuart H Orkin; B G Forget; David G Nathan
Prenatal diagnosis of hemoglobinopathies: the New England approach.
Annals of the New York Academy of Sciences 1980;344():151-64.
1980: BLANCHE ALTER; S C Goff; T J Klonowski; M D Garrick
Chemical evidence for the separation of G gamma and A gamma chains by polyacrylamide gel electrophoresis in urea and triton X-100.
Preparative biochemistry 1980;10(5):633-44.
1980: D G Nathan; BLANCHE ALTER
F-cell regulation.
Annals of the New York Academy of Sciences 1980;344():219-32.
1979: BLANCHE ALTER
The G gamma:A gamma composition of fetal hemoglobin in fetuses and newborns.
Blood 1979;54(5):1158-63.
1979: B J Clarke; D G Nathan; BLANCHE ALTER; B G Forget; D G Hillman; D Housman
Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies.
Blood 1979;54(4):805-17.
1979: BLANCHE ALTER
Prenatal diagnosis of hemoglobinopathies and other hematologic diseases.
The Journal of pediatrics 1979;95(4):501-3.
1979: S H Orkin; BLANCHE ALTER; C Altay
Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
The Journal of clinical investigation 1979;64(3):866-9.
1979: David G Nathan; BLANCHE ALTER; Stuart H Orkin
Prenatal diagnosis of hemoglobinopathies.
Clinics in perinatology 1979;6(2):275-91.
1979: BLANCHE ALTER
Bone-marrow failure in children.
Pediatric annals 1979;8(7):444-57.
1979: BLANCHE ALTER; D G Nathan
Red cell aplasia in children.
Archives of disease in childhood 1979;54(4):263-7.
1979: BLANCHE ALTER; J B Metzger; P G Yock; S B Rothchild; George J Dover
Selective hemolysis of adult red blood cells: an aid to prenatal diagnosis of hemoglobinopathies.
Blood 1979;53(2):279-87.
1979: BLANCHE ALTER
Fetal erythropoiesis in stress hematopoiesis.
Experimental hematology 1979;7 Suppl 5():200-9.
1978: BLANCHE ALTER; S C Goff
Variable globin chain synthesis in mouse erythroleukemia cells.
Blood 1978;52(5):1047-57.
1978: BLANCHE ALTER
Thumbs and anemia.
Pediatrics 1978;62(4):613-4.
1978: BLANCHE ALTER; N U Potter; Frederick P Li
Classification and aetiology of the aplastic anaemias.
Clinics in haematology 1978;7(3):431-65.
1978: Stuart H Orkin; BLANCHE ALTER; C Altay; M J Mahoney; H Lazarus; J C Hobbins; David G Nathan
Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion.
The New England journal of medicine 1978;299(4):166-72.
1978: D G Nathan; D G Hillman; L Chess; BLANCHE ALTER; B J Clarke; J Breard; D E Housman
Normal erythropoietic helper T cells in congenital hypoplastic (Diamond-Blackfan) anemia.
The New England journal of medicine 1978;298(19):1049-51.
1978: BLANCHE ALTER
Beta-thalassaemia trait: imprecision of diagnosis at birth.
British journal of haematology 1978;38(3):323-7.
1978: D V Fairweather; B Modell; V Berdoukas; BLANCHE ALTER; D G Nathan; DIMITRIS LOUKOPOULOS; W Wood; J B Clegg; D J Weatherall
Antenatal diagnosis of thalassaemia major.
British medical journal 1978;1(6109):350-3.
1978: D G Nathan; B J Clarke; D G Hillman; BLANCHE ALTER; D E Housman
Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia.
The Journal of clinical investigation 1978;61(2):489-98.
1978: BLANCHE ALTER; D G Nathan
Antenatal diagnosis of haematological disorders--'1978'.
Clinics in haematology 1978;7(1):195-216.
1978: W C Wang; W Mentzer; BLANCHE ALTER
Congenital hypoplastic anemia: Diamond-Blackfan syndrome. Comments and additional data on clinical aspects of Diamond-Blackfan syndrome.
Blood cells 1978;4(1-2):215-8.
1977: BLANCHE ALTER; S C Goff
Globin synthesis in mouse erythroleukemia cells in vitro: a switch in beta chains due to inducing agent.
Blood 1977;50(5):867-76.
1977: BLANCHE ALTER; S C Goff; D G Hillman; A B Deisseroth; B G Forget
Production of mouse globin in heterokaryons of mouse erythroleukaemia cells and human fibroblasts.
Journal of cell science 1977;26():347-57.
1977: BLANCHE ALTER; D G Nathan; C B Modell; D Fairweather; M J Mahoney; J C Hobbins
Prenatal diagnosis of hemoglobinopathies: detection of alpha-thalassemia trait and of sickle cell disease in utero.
Hemoglobin 1977;1(4):395-400.
1976: BLANCHE ALTER; C B Modell; D Fairweather; J C Hobbins; M J Mahoney; F D Frigoletto; A S Sherman; D G Nathan
Prenatal diagnosis of hemoglobinopathies. A review of 15 cases.
The New England journal of medicine 1976;295(26):1437-43.
1976: BLANCHE ALTER; J M Rappeport; T H Huisman; W A Schroeder; D G Nathan
Fetal erythropoiesis following bone marrow transplantation.
Blood 1976;48(6):843-53.
1976: BLANCHE ALTER; S Friedman; J C Hobbins; M J Mahoney; A S Sherman; J F McSweeney; D G Nathan; E Schwartz
Prenatal diagnosis of sickle-cell anemia and alpha G Philadelphia. Study of a Fetus also at risk for H b S/beta+-thalassemia.
The New England journal of medicine 1976;294(19):1040-1.
1976: L K Diamond; W C Wang; BLANCHE ALTER
Congenital hypoplastic anemia.
Advances in pediatrics 1976;22():349-78.
1975: H Chang; C B Modell; BLANCHE ALTER; M J Dickinson; F D Frigoletto; E R Huehns; D G Nathan
Expression of the beta-thalassemia gene in the first trimester fetus.
Proceedings of the National Academy of Sciences of the United States of America 1975;72(9):3633-7.
1975: D G Nathan; BLANCHE ALTER; F D Frigoletto
Antenatal diagnosis of hemoglobinopathies: social and technical considerations.
Seminars in hematology 1975;12(3):305-21.
1975: BLANCHE ALTER; Vernon M Ingram
Globin synthesis in fibroblasts fused with erythroblasts. I. Avian fibroblasts.
Somatic cell genetics 1975;1(2):165-85.
1974: BLANCHE ALTER; Y W Kan; D G Nathan
Toxic effects of high-dose cyanate administration in rodents.
Blood 1974;43(1):69-77.
1974: BLANCHE ALTER; Y W Kan; D G Nathan
Inhibition of hemoglobin synthesis by cyanate in vitro.
Blood 1974;43(1):57-68.
1972: BLANCHE ALTER; Y W Kan; D G Nathan
Reticulocyte survival in sickle cell anemia: effect of cyanate.
Blood 1972;40(5):733-9.
1972: Frederick P Li; BLANCHE ALTER; D G Nathan
The mortality of acquired aplastic anemia in children.
Blood 1972;40(2):153-62.
1972: Y W Kan; A M Dozy; BLANCHE ALTER; F D Frigoletto; D G Nathan
Detection of the sickle gene in the human fetus. Potential for intrauterine diagnosis of sickle-cell anemia.
The New England journal of medicine 1972;287(1):1-5.
1970: BLANCHE ALTER
Systemic lupus erythematosus and ethosuccimide.
The Journal of pediatrics 1970;77(6):1093-5.
1968: BLANCHE ALTER; E E Czapek; R D Rowe
Sweating in congenital heart disease.
Pediatrics 1968;41(1):123-9.