Daniel Van Dyke

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Dewald Gordon W; Smyrk Thomas C; Thorland Erik C; McWilliams Robert R; Van Dyke Daniel L; Keefe Jeannette G; Belongie Kimberly J; Smoley Stephanie A; Knutson Darlene L; Fink Stephanie R; Wiktor Anne E; Petersen Gloria M
Fluorescence in situ hybridization to visualize genetic abnormalities in interphase cells of acinar cell carcinoma, ductal adenocarcinoma, and islet cell carcinoma of the pancreas.
Wiktor Anne E; Hanson Curtis A; Hodnefield Janice M; Hussein Kebede; Tefferi Ayalew; Van Dyke Daniel L
Circulating blasts or myeloid precursor cells in peripheral blood can predict success of cytogenetic analysis.
Fink Stephanie R; Belongie Kimberly J; Paternoster Sarah F; Smoley Stephanie A; Pardanani Animesh D; Tefferi Ayalew; Van Dyke Daniel L; Ketterling Rhett P
Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations.

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2009: Dewald Gordon W; Smyrk Thomas C; Thorland Erik C; McWilliams Robert R; Van Dyke Daniel L; Keefe Jeannette G; Belongie Kimberly J; Smoley Stephanie A; Knutson Darlene L; Fink Stephanie R; Wiktor Anne E; Petersen Gloria M
Fluorescence in situ hybridization to visualize genetic abnormalities in interphase cells of acinar cell carcinoma, ductal adenocarcinoma, and islet cell carcinoma of the pancreas.
Mayo Clinic proceedings. Mayo Clinic 2009;84(9):801-10.
2009: Wiktor Anne E; Hanson Curtis A; Hodnefield Janice M; Hussein Kebede; Tefferi Ayalew; Van Dyke Daniel L
Circulating blasts or myeloid precursor cells in peripheral blood can predict success of cytogenetic analysis.
Leukemia research 2009;33(7):e75-6.
2009: Fink Stephanie R; Belongie Kimberly J; Paternoster Sarah F; Smoley Stephanie A; Pardanani Animesh D; Tefferi Ayalew; Van Dyke Daniel L; Ketterling Rhett P
Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations.
Leukemia research 2009;33(6):843-6.
2009: Hussein Kebede; Van Dyke Daniel L; Tefferi Ayalew
Conventional cytogenetics in myelofibrosis: literature review and discussion.
European journal of haematology 2009;82(5):329-38.
2009: Hussein Kebede; Huang Jocelin; Lasho Terra; Pardanani Animesh; Mesa Ruben A; Williamson Cynthia M; Ketterling Rhett P; Hanson Curtis A; Van Dyke Daniel L; Tefferi Ayalew
Karyotype complements the International Prognostic Scoring System for primary myelofibrosis.
European journal of haematology 2009;82(4):255-9.
2009: Wiktor Anne E; Bender Grant; Van Dyke Daniel L
Identification of sex chromosome mosaicism: is analysis of 20 metaphase cells sufficient?
American journal of medical genetics. Part A 2009;149A(2):257-9.
2008: Hussein Kebede; Ketterling Rhett P; Dewald Gordon W; Van Dyke Daniel L; Mesa Ruben; Hanson Curtis A; Tefferi Ayalew
Peripheral blood cytogenetic studies in myelofibrosis: overall yield and comparison with bone marrow cytogenetic studies.
Leukemia research 2008;32(10):1597-600.
2008: Hussein Kebede; Ketterling Rhett P; Hulshizer Rachael L; Kuffel Daniel G; Wiktor Anne E; Hanson Curtis A; Tefferi Ayalew; Van Dyke Daniel L
Peripheral blood cytogenetic studies in hematological neoplasms: predictors of obtaining metaphases for analysis.
European journal of haematology 2008;80(4):318-21.
2008: Hanson Curtis A; Steensma David P; Hodnefield Janice M; Nguyen Phuong L; Hoyer James D; Viswanatha David S; Zou Ying; Knudson Ryan A; Van Dyke Daniel L; Ketterling Rhett P
Isolated trisomy 15: a clonal chromosome abnormality in bone marrow with doubtful hematologic significance.
American journal of clinical pathology 2008;129(3):478-85.
2007: Bowen Deborah A; Call Timothy G; Jenkins Greg D; Zent Clive S; Schwager Susan M; Van Dyke Daniel L; Jelinek Diane F; Kay Neil E; Shanafelt Tait D
Methylprednisolone-rituximab is an effective salvage therapy for patients with relapsed chronic lymphocytic leukemia including those with unfavorable cytogenetic features.
Leukemia & lymphoma 2007;48(12):2412-7.
2007: Adeyinka Adewale; Smoley Stephanie; Fink Stephanie; Sanchez Jessica; Van Dyke Daniel L; Dewald Gordon
Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns.
Cancer genetics and cytogenetics 2007;179(1):25-30.
2007: Ida Cristiane M; Rolig Kristen A; Hulshizer Rachael L; Van Dyke Daniel L; Randolph Jamie L; Jenkins Robert B; Nascimento Antonio G; Oliveira Andre M
Myxoinflammatory fibroblastic sarcoma showing t(2;6)(q31;p21.3) as a sole cytogenetic abnormality.
Cancer genetics and cytogenetics 2007;177(2):139-42.
2007: Micale Mark A; Schran David; Emch Sean; Kurczynski Thaddeus W; Rahman Nazneen; Van Dyke Daniel L
Mosaic variegated aneuploidy without microcephaly: implications for cytogenetic diagnosis.
American journal of medical genetics. Part A 2007;143A(16):1890-3.
2007: Van Dyke D L; Ebrahim S A; Al Saadi A A; Powell S A; Zenger-Hain J L; Micale M A; Wiktor A E; Zou Y S
The impact of maternal serum screening programs for Down syndrome in southeast Michigan, 1988-2003.
Prenatal diagnosis 2007;27(6):583-4.
2007: Zou Ying S; Van Dyke Daniel L; Ellison Jay W
Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems.
American journal of medical genetics. Part A 2007;143(7):746-51.
2006: Graf M D; Christ L; Mascarello J T; Mowrey P; Pettenati M; Stetten G; Storto P; Surti U; Van Dyke D L; Vance G H; Wolff D; Schwartz S
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
Journal of medical genetics 2006;43(8):660-4.
2006: Zou Ying S; Van Dyke Daniel L; Thorland Erik C; Chhabra Harinderpal S; Michels Virginia V; Keefe Jeannette G; Lega Melanie A; Feely Molly A; Uphoff Timothy S; Jalal Syed M
Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review.
American journal of medical genetics. Part A 2006;140(15):1696-706.
2006: Zou Ying S; McGrann Pamela S; Uphoff Timothy S; Van Dyke Daniel L
A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14.
American journal of medical genetics. Part A 2006;140(15):1663-8.
2006: Fink Stephanie R; Smoley Stephanie A; Stockero Kimberly J; Paternoster Sarah F; Thorland Erik C; Van Dyke Daniel L; Shanafelt Tait D; Zent Clive S; Call Timothy G; Kay Neil E; Dewald Gordon W
Loss of TP53 is due to rearrangements involving chromosome region 17p10 approximately p12 in chronic lymphocytic leukemia.
Cancer genetics and cytogenetics 2006;167(2):177-81.
2006: Lebel Robert Roger; Roberson Jacquelyn; Van Dyke Daniel L
Regarding trisomy 18.
American journal of medical genetics. Part A 2006;140(9):964-5.
2006: Stockero Kimberly J; Fink Stephanie R; Smoley Stephanie A; Paternoster Sarah F; Shanafelt Tait D; Call Timothy G; Zent Clive S; Van Dyke Daniel L; Kay Neil E; Dewald Gordon W
Metaphase cells with normal G-bands have cryptic interstitial deletions in 13q14 detectable by fluorescence in situ hybridization in B-cell chronic lymphocytic leukemia.
Cancer genetics and cytogenetics 2006;166(2):152-6.
2006: Wiktor Anne E; Van Dyke Daniel L; Stupca Peggy J; Ketterling Rhett P; Thorland Erik C; Shearer Brandon M; Fink Stephanie R; Stockero Kimberly J; Majorowicz Jason R; Dewald Gordon W
Preclinical validation of fluorescence in situ hybridization assays for clinical practice.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(1):16-23.
2006: Welch Robert A; Salem-Elgharib Soha; Wiktor Anne E; Van Dyke Daniel L; Blessed William B
Operator experience and sample quality in genetic amniocentesis.
American journal of obstetrics and gynecology 2006;194(1):189-91.
2005: Dewald Gordon W; Therneau Terry; Larson Dirk; Lee You Kyoung; Fink Stephanie; Smoley Stephanie; Paternoster Sarah; Adeyinka Adewale; Ketterling Rhett; Van Dyke Daniel L; Fonseca Rafael; Kyle Robert
Relationship of patient survival and chromosome anomalies detected in metaphase and/or interphase cells at diagnosis of myeloma.
Blood 2005;106(10):3553-8.
2005: Wiktor Anne E; Van Dyke Daniel L
Detection of low level sex chromosome mosaicism in Ullrich-Turner syndrome patients.
American journal of medical genetics. Part A 2005;138A(3):259-61.
2005: Adeyinka Adewale; Adams S Annie; Lorentz Cindy P; Van Dyke Daniel L; Jalal Syed M
Subtelomere deletions and translocations are frequently familial.
American journal of medical genetics. Part A 2005;135(1):28-35.
2005: Caudill Samuel P; Van Dyke Daniel L; Chen Andrew T L; Reidy John A; Ing Paul S; Schwartz Stuart; Vance Gail H
Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices.
Statistics in medicine 2005;24(4):615-22.
2004: Wiktor Anne; Van Dyke Daniel L
Combined cytogenetic testing and fluorescence in situ hybridization analysis in the study of chronic lymphocytic leukemia and multiple myeloma.
Cancer genetics and cytogenetics 2004;153(1):73-6.
2004: Coon Steven W; Savera Adnan T; Zarbo Richard J; Benninger Michael S; Chase Gary A; Rybicki Benjamin A; Van Dyke Daniel L
Prognostic implications of loss of heterozygosity at 8p21 and 9p21 in head and neck squamous cell carcinoma.
International journal of cancer. Journal international du cancer 2004;111(2):206-12.
2004: Zhang Yanming; Emmanuel Neelmini; Kamboj Ginny; Chen Jianjun; Shurafa Muhammad; Van Dyke Daniel L; Wiktor Anne; Rowley Janet D
PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22).
Genes, chromosomes & cancer 2004;40(4):365-70.
2004: Wiktor Anne; Van Dyke Daniel L
FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients.
Genetics in medicine : official journal of the American College of Medical Genetics 2004;6(3):132-5.
2004: Asamoah Alexnder; Nwankwo Martin; Kumar Savitri P; Ezhuthachan Sudhakar G; Van Dyke Daniel L
Proximal chromosome 8q deletion in a boy with femoral bifurcation and other multiple congenital anomalies.
American journal of medical genetics. Part A 2004;127A(1):65-8.
2004: Kuriakose Philip; Perveen Nusrat; Maeda Koichi; Wiktor Anne; Van Dyke Daniel L
Translocation (8;14)(q24;q32) as the sole cytogenetic abnormality in B-cell prolymphocytic leukemia.
Cancer genetics and cytogenetics 2004;150(2):156-8.
2004: Raitanen Misa; Worsham Maria J; Lakkala Taina; Carey Thomas E; Van Dyke Daniel L; Grénman Reidar; Klemi Pekka; Rantanen Virpi; Isola Jorma; Grénman Seija
Characterization of 10 vulvar carcinoma cell lines by karyotyping, comparative genomic hybridization and flow cytometry.
Gynecologic oncology 2004;93(1):155-63.
2003: Rybicki Benjamin A; Savera Adnan T; Gomez Jose A; Patel Sonal C; Ballard Nicole E; Benninger Michael S; Zarbo Richard J; Van Dyke Daniel L
Allelic loss and tumor pathology in head and neck squamous cell carcinoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2003;16(10):970-9.
2003: Van Dyke Daniel L; Wiktor Anne
Monosomy 21 in hematologic diseases.
Cancer genetics and cytogenetics 2003;142(2):137-41.
2003: Asamoah Alexander; Decker Amy B; Wiktor Anne; Van Dyke Daniel L
Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay.
American journal of medical genetics. Part A 2003;118A(1):82-5.
2002: Monaghan Kristin G; Wiktor Anne; Van Dyke Daniel L
Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: a cost comparison.
Genetics in medicine : official journal of the American College of Medical Genetics 2002;4(6):448-50.
2002: Wilson Susan Clement; Susman Marleen; Bain Sharon; Wohlferd Monica; Van Dyke Daniel L; Daniel Art; White Beverly; Gardner R J McKinlay
Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.
Prenatal diagnosis 2002;22(8):681-5.
2001: Satinover D L; Vance G H; Van Dyke D L; Schwartz S
Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.
Chromosoma 2001;110(4):275-83.
2001: Wiktor A; Feldman G L; Bawle E V; Czarnecki P; Conard J V; Van Dyke D L
Deletion of 2q37 and duplication of 10q24: two cases in the same family and review of the literature.
Annales de génétique 2001;44(3):129-34.
2001: Manji S; Roberson J R; Wiktor A; Vats S; Rush P; Diment S; Van Dyke D L
Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(1):65-6.
2001: Barnabas N; Shurafa M; Van Dyke D L; Wolman S R; Clark D; Worsham M J
Significance of p53 mutations in patients with chronic lymphocytic leukemia: a sequential study of 30 patients.
Cancer 2001;91(2):285-93.
2000: Teshima I; Bawle E V; Weksberg R; Shuman C; Van Dyke D L; Schwartz S
Analphoid 3qter markers.
American journal of medical genetics 2000;94(2):113-9.
2000: Baumgartner B J; Shurafa M; Terebelo H; Tapazoglou E; Van Dyke D L
Trisomy 15, sex chromosome loss, and hematological malignancy.
Cancer genetics and cytogenetics 2000;117(2):132-5.
2000: Wallerstein R; Yu M T; Neu R L; Benn P; Lee Bowen C; Crandall B; Disteche C; Donahue R; Harrison B; Hershey D; Higgins R R; Jenkins L S; Jackson-Cook C; Keitges E; Khodr G; Lin C C; Luthardt F W; Meisner L; Mengden G; Patil S R; Rodriguez M; Sciorra L J; Shaffer L G; Stetten G; Van Dyke D L; Wang H
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
Prenatal diagnosis 2000;20(2):103-22.
2000: Wiktor A; Rybicki B A; Piao Z S; Shurafa M; Barthel B; Maeda K; Van Dyke D L
Clinical significance of Y chromosome loss in hematologic disease.
Genes, chromosomes & cancer 2000;27(1):11-6.
1999: Ing P S; Van Dyke D L; Caudill S P; Reidy J A; Bice G; Bieber F R; Buchanan P D; Carroll A J; Cheung S W; DeWald G; Donahue R P; Gardner H A; Higgins J; Hsu L Y; Jamehdor M; Keitges E A; Laundon C H; Luthardt F W; Mascarello J; May K M; Meck J M; Morton C; Patil S; Peakman D; Pettenati M J; Rao N; Sanger W G; Saxe D F; Schwartz S; Sekhon G S; Vance G H; Wyandt H E; Yu C W; Zenger-Hain J; Chen A T
Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.
Genetics in medicine : official journal of the American College of Medical Genetics 1999;1(3):94-7.
1999: Worsham M J; Wolman S R; Carey T E; Zarbo R J; Benninger M S; Van Dyke D L
Chromosomal aberrations identified in culture of squamous carcinomas are confirmed by fluorescence in situ hybridisation.
Molecular pathology : MP 1999;52(1):42-6.
1999: Tsai C H; Van Dyke D L; Feldman G L
Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.
American journal of medical genetics 1999;82(4):336-9.
1999: Berend S A; Feldman G L; McCaskill C; Czarnecki P; Van Dyke D L; Shaffer L G
Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.
American journal of medical genetics 1999;82(3):275-81.
1998: Zinn A R; Tonk V S; Chen Z; Flejter W L; Gardner H A; Guerra R; Kushner H; Schwartz S; Sybert V P; Van Dyke D L; Ross J L
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
American journal of human genetics 1998;63(6):1757-66.
1998: Chen A T; Ing P S; Reidy J A; Schwartz S; Vance G H; Van Dyke D L
The ACMG CYTO2000 subcommittee?
Genetics in medicine : official journal of the American College of Medical Genetics 1998;1(1):67.
1998: Monaghan K G; Van Dyke D L; Feldman G L
Prader-Willi-like syndrome in a patient with an Xq23q25 duplication.
American journal of medical genetics 1998;80(3):227-31.
1998: Pratt V M; Roberson J R; Weiss L; Van Dyke D L
Duplication 6q21q23 in two unrelated patients.
American journal of medical genetics 1998;80(2):112-4.
1998: Bawle E V; Conard J; Van Dyke D L; Czarnecki P; Driscoll D A
Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case.
American journal of medical genetics 1998;79(5):406-10.
1998: Wiktor A; Puskorius R; Zubrickas K; Van Dyke D L
Sequential G-banding and fluorescent in situ hybridization on peripheral blood, bone marrow, and amniotic fluid samples.
American journal of medical genetics 1998;79(1):38-41.
1998: White W M; Willard H F; Van Dyke D L; Wolff D J
The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA.
American journal of human genetics 1998;63(1):20-8.
1998: Czarnecki P M; Van Dyke D L; Vats S; Feldman G L
A mother with VCFS and unilateral dysplastic kidney and her fetus with multicystic dysplastic kidneys: additional evidence to support the association of renal malformations and VCFS.
Journal of medical genetics 1998;35(4):348.
1997: Monaghan K G; Van Dyke D L; Wiktor A; Feldman G L
Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.
American journal of medical genetics 1997;73(2):180-3.
1997: Depinet T W; Zackowski J L; Earnshaw W C; Kaffe S; Sekhon G S; Stallard R; Sullivan B A; Vance G H; Van Dyke D L; Willard H F; Zinn A B; Schwartz S
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.
Human molecular genetics 1997;6(8):1195-204.
1997: Wolff D J; Gustashaw K M; Zurcher V; Ko L; White W; Weiss L; Van Dyke D L; Schwartz S; Willard H F
Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern.
Human genetics 1997;100(2):256-61.
1997: Jones J W; Raval J R; Beals T F; Worsham M J; Van Dyke D L; Esclamado R M; Wolf G T; Bradford C R; Miller T; Carey T E
Frequent loss of heterozygosity on chromosome arm 18q in squamous cell carcinomas. Identification of 2 regions of loss--18q11.1-q12.3 and 18q21.1-q23.
Archives of otolaryngology--head & neck surgery 1997;123(6):610-4.
1997: Hsu L Y; Yu M T; Neu R L; Van Dyke D L; Benn P A; Bradshaw C L; Shaffer L G; Higgins R R; Khodr G S; Morton C C; Wang H; Brothman A R; Chadwick D; Disteche C M; Jenkins L S; Kalousek D K; Pantzar T J; Wyatt P
Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.
Prenatal diagnosis 1997;17(3):201-42.
1997: Monaghan K G; Van Dyke D L; Feldman G; Wiktor A; Weiss L
Diagnostic testing: a cost analysis for Prader-Willi and Angelman syndromes.
American journal of human genetics 1997;60(1):244-7.
1997: Carey T E; Frank C J; Raval J R; Jones J W; McClatchey K D; Beals T F; Worsham M J; Van Dyke D L
Identifying genetic changes associated with tumor progression in squamous cell carcinoma.
Acta oto-laryngologica. Supplementum 1997;529():229-32.
1996: Kelker W; Van Dyke D L; Worsham M J; Christopherson P L; James C D; Conlon M R; Carey T E
Loss of 18q and homozygosity for the DCC locus: possible markers for clinically aggressive squamous cell carcinoma.
Anticancer research 1996;16(4C):2365-72.
1996: Hsu L Y; Yu M T; Richkind K E; Van Dyke D L; Crandall B F; Saxe D F; Khodr G S; Mennuti M; Stetten G; Miller W A; Priest J H
Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
Prenatal diagnosis 1996;16(1):1-28.
1996: Wolff D J; Miller A P; Van Dyke D L; Schwartz S; Willard H F
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
American journal of human genetics 1996;58(1):154-60.
1995: Bischoff F Z; Zenger-Hain J; Moses D; Van Dyke D L; Shaffer L G
Mosaicism for trisomy 12: four cases with varying outcomes.
Prenatal diagnosis 1995;15(11):1017-26.
1995: Scheuerle A; Zenger-Hain J L; Van Dyke D L; Ledbetter D H; Greenberg F; Shaffer L G
Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).
American journal of medical genetics 1995;56(4):403-8.
1995: Worsham M J; Wolman S R; Carey T E; Zarbo R J; Benninger M S; Van Dyke D L
Common clonal origin of synchronous primary head and neck squamous cell carcinomas: analysis by tumor karyotypes and fluorescence in situ hybridization.
Human pathology 1995;26(3):251-61.
1994: Shaffer L G; McCaskill C; Han J Y; Choo K H; Cutillo D M; Donnenfeld A E; Weiss L; Van Dyke D L
Molecular characterization of de novo secondary trisomy 13.
American journal of human genetics 1994;55(5):968-74.
1994: Wiktor A; Feldman G L; Kratkoczki P; Ditmars D M; Van Dyke D L
10p duplication characterized by fluorescence in situ hybridization.
American journal of medical genetics 1994;52(3):315-8.
1994: Jalal S M; Law M E; Dewald G W; Sekhor G S; Van Dyke D L
Detection of 46,XX male by Y-specific whole chromosome paint probe.
American journal of medical genetics 1994;52(2):239-41.
1994: Van Dyke D L; Worsham M J; Benninger M S; Krause C J; Baker S R; Wolf G T; Drumheller T; Tilley B C; Carey T E
Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region.
Genes, chromosomes & cancer 1994;9(3):192-206.
1993: Zenger-Hain J L; Van Dyke D L; Wiktor A; Walker H; Feldman G L
Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
American journal of medical genetics 1993;47(8):1198-201.
1993: Migeon B R; Luo S; Stasiowski B A; Jani M; Axelman J; Van Dyke D L; Weiss L; Jacobs P A; Yang-Feng T L; Wiley J E
Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(24):12025-9.
1993: Carey T E; Van Dyke D L; Worsham M J
Nonrandom chromosome aberrations and clonal populations in head and neck cancer.
Anticancer research 1993;13(6B):2561-7.
1993: Zenger-Hain J L; Wiktor A; Goldman J; Van Dyke D L; Weiss L
X-inactivation pattern in an Ullrich-Turner syndrome patient with a small ring X and normal intelligence.
American journal of medical genetics 1993;47(4):490-3.
1993: Feldman G L; Weiss L; Phelan M C; Schroer R J; Van Dyke D L
Inverted duplication of 8p: ten new patients and review of the literature.
American journal of medical genetics 1993;47(4):482-6.
1993: Worsham M J; Carey T E; Benninger M S; Gasser K M; Kelker W; Zarbo R J; Van Dyke D L
Clonal cytogenetic evolution in a squamous cell carcinoma of the skin from a xeroderma pigmentosum patient.
Genes, chromosomes & cancer 1993;7(3):158-64.
1993: Zenger-Hain J L; Roberson J; Van Dyke D L; Weiss L
Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
American journal of medical genetics 1993;46(4):438-40.
1993: Wiktor A; Van Dyke D L; Weiss L
Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).
American journal of medical genetics 1993;45(1):22-4.
1993: Worsham M J; Benninger M J; Zarbo R J; Carey T E; Van Dyke D L
Deletion 9p22-pter and loss of Y as primary chromosome abnormalities in a squamous cell carcinoma of the vocal cord.
Genes, chromosomes & cancer 1993;6(1):58-60.
1993: Carey T E; Worsham M J; Van Dyke D L
Chromosomal biomarkers in the clonal evolution of head and neck squamous neoplasia.
Journal of cellular biochemistry. Supplement 1993;17F():213-22.
1992: Van Dyke D L; Wiktor A; Palmer C G; Miller D A; Witt M; Babu V R; Worsham M J; Roberson J R; Weiss L
Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation.
American journal of medical genetics 1992;43(6):996-1005.
1992: Falik-Borenstein T C; Pribyl T M; Pulst S M; Van Dyke D L; Weiss L; Chu M L; Kraus J; Marshak D; Korenberg J R
Stable ring chromosome 21: molecular and clinical definition of the lesion.
American journal of medical genetics 1992;42(1):22-8.
1991: Worsham M J; Van Dyke D L; Grenman S E; Grenman R; Hopkins M P; Roberts J A; Gasser K M; Schwartz D R; Carey T E
Consistent chromosome abnormalities in squamous cell carcinoma of the vulva.
Genes, chromosomes & cancer 1991;3(6):420-32.
1991: Bradford C R; Kimmel K A; Van Dyke D L; Worsham M J; Tilley B J; Burk D; del Rosario F; Lutz S; Tooley R; Hayashida D J
11p deletions and breakpoints in squamous cell carcinoma: association with altered reactivity with the UM-E7 antibody.
Genes, chromosomes & cancer 1991;3(4):272-82.
1991: Tazelaar J; Roberson J; Van Dyke D L; Babu V R; Weiss L
Mother and son with deletion of 3p25-pter.
American journal of medical genetics 1991;39(2):130-2.
1991: Van Dyke D L; Wiktor A; Roberson J R; Weiss L
Mental retardation in Turner syndrome.
The Journal of pediatrics 1991;118(3):415-7.
1990: Babu V R; Miles B J; Cerny J C; Weiss L; Van Dyke D L
Cytogenetic study of four cancers of the prostate.
Cancer genetics and cytogenetics 1990;48(1):83-7.
1990: Bodrug S E; Roberson J R; Weiss L; Ray P N; Worton R G; Van Dyke D L
Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.
Journal of medical genetics 1990;27(7):426-32.
1990: Nowinski G P; Van Dyke D L; Tilley B C; Jacobsen G; Babu V R; Worsham M J; Wilson G N; Weiss L
The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history.
American journal of human genetics 1990;46(6):1101-11.
1990: Grenman S E; Worsham M J; Van Dyke D L; England B; McClatchey K D; Babu V R; Roberts J A; Mäenpää J; Carey T E
Establishment and characterization of UM-EC-2, a tamoxifen-sensitive, estrogen receptor-negative human endometrial carcinoma cell line.
Gynecologic oncology 1990;37(2):188-99.
1990: Grénman S E; Van Dyke D L; Worsham M J; England B; McClatchey K D; Hopkins M; Babu V R; Grénman R; Carey T E
Phenotypic characterization, karyotype analysis and in vitro tamoxifen sensitivity of new ER-negative vulvar carcinoma cell lines, UM-SCV-1A and UM-SCV-1B.
International journal of cancer. Journal international du cancer 1990;45(5):920-7.
1990: Raman B K; Janakiraman N; Raju U R; Carey J; Babu V R; Van Dyke D L; Van Slyck E J
Osteomyelosclerosis with granulocytic sarcoma of chest wall. Morphological, ultrastructural, immunologic, and cytogenetic study.
Archives of pathology & laboratory medicine 1990;114(4):426-9.
1989: Carey T E; Van Dyke D L; Worsham M J; Bradford C R; Babu V R; Schwartz D R; Hsu S; Baker S R
Characterization of human laryngeal primary and metastatic squamous cell carcinoma cell lines UM-SCC-17A and UM-SCC-17B.
Cancer research 1989;49(21):6098-107.
1989: Van Dyke D L; Roberson J R; Babu V R; Weiss L; Tyrkus M
Trisomy 20 mosaicism identified prenatally and confirmed in foreskin fibroblasts.
Prenatal diagnosis 1989;9(8):601-2.
1989: Robinow M; Haney N; Chen H; Sorauf T; Van Dyke D L; Babu V R; Powell S; Maliszewski W; Guerin S; Landers J W
Secondary trisomy or mosaic "tetrasomy" 8p.
American journal of medical genetics 1989;32(3):320-4.
1989: Babu V R; Miles B J; Cerney J C; Weiss L; van Dyke D L
Chromosome 21q22 deletion. A specific chromosome change in a new bladder cancer subgroup.
Cancer genetics and cytogenetics 1989;38(1):127-9.
1989: Van Dyke D L; Marcy A; Craig B M; Babu V R; Roberson J R
Chromosome 1 deletion associated with increased nuchal fold thickness in the second trimester.
Prenatal diagnosis 1989;9(2):141-2.
1989: Worsham M J; Miller D A; Devries J M; Mitchell A R; Babu V R; Surli V; Weiss L; Van Dyke D L
A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres.
American journal of human genetics 1989;44(1):115-23.
1989: Jackson C E; Van Dyke D L; Talpos G B; Norum R A; Tashjian A H
MEN-2 tumor associations suggest a linear order of specific endocrine tumor genes.
Hormone and metabolic research. Supplement series 1989;21():9-12.
1988: Flejter W L; Babu V R; Van Dyke D L; Jackson C E
High-resolution studies of chromosome 10 in 23 MEN-2 families.
Cancer genetics and cytogenetics 1988;32(2):301-3.
1988: Grenman S E; Van Dyke D L; Worsham M J; del Rosario F; Roberts J A; McClatchey K D; Schwartz D R; Babu V R; Carey T E
UM-EC-1, a new hypodiploid human cell line derived from a poorly differentiated endometrial cancer.
Cancer research 1988;48(7):1864-73.
1988: Forsythe M G; Walker H; Weiss L; Roberson J R; Worsham M J; Babu V R; Van Dyke D L
Duplication and deletion 11q23-q24 recombinants in two offspring of an intrachromosomal insertion ("shift") carrier.
Henry Ford Hospital medical journal 1988;36(4):183-6.
1987: Babu V R; Lutz M D; Miles B J; Farah R N; Weiss L; Van Dyke D L
Tumor behavior in transitional cell carcinoma of the bladder in relation to chromosomal markers and histopathology.
Cancer research 1987;47(24 Pt 1):6800-5.
1987: Van Dyke D L; Worsham M; Weiss L
The human inactivated X chromosome folds in early metaphase, prometaphase, and prophase.
Human genetics 1987;77(1):57-9.
1987: Van Dyke D L; Babu V R; Weiss L
Parental age, and how extra isochromosomes (secondary trisomy) arise.
Clinical genetics 1987;32(1):75-9.
1987: Babu V R; Van Dyke D L; Flejter W L; Jackson C E
Chromosome 20 deletion in multiple endocrine neoplasia type 2: expanded double-blind studies.
American journal of medical genetics 1987;27(3):739-48.
1987: Kurtzman D N; Van Dyke D L; Rich C A; Weiss L
Duplication 3p21----3pter and cyclopia.
American journal of medical genetics 1987;27(1):33-7.
1987: Gaba A R; Van Dyke D L; Weiss L
Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant.
American journal of medical genetics 1987;26(3):545-9.
1986: Stoffer S S; Van Dyke D L; Bach J V; Szpunar W; Weiss L
Familial papillary carcinoma of the thyroid.
American journal of medical genetics 1986;25(4):775-82.
1986: Flejter W L; Van Dyke D L; Weiss L
Location of the X inactivation center in primates and other mammals.
Human genetics 1986;74(1):63-6.
1986: Maeda K; Hawkins E T; Oh H K; Kini S R; Van Dyke D L
Malignant lymphoma in transplanted renal pelvis.
Archives of pathology & laboratory medicine 1986;110(7):626-9.
1986: Van Dyke D L; Flejter W L; Worsham M J; Roberson J R; Higgins J V; Herr H M; Knuutila S; Wang N; Babu V R; Weiss L
A practical metaphase marker of the inactive X chromosome.
American journal of human genetics 1986;39(1):88-95.
1986: Van Dyke D L; Worsham M J; Fisher L J; Weiss L
The centromere index and relative length of human high-resolution G-banded chromosomes.
Human genetics 1986;73(2):130-2.
1986: Van Dyke D L; Weiss L
Maternal effect on intelligence in fragile X males and females.
American journal of medical genetics 1986;23(1-2):723-37.
1984: Stanley W S; Barr M; Hensinger R; Ruby S G; Van Dyke D L; Weiss L
Asymmetric skeletal anomalies in siblings.
Clinical genetics 1984;25(6):533-7.
1984: Babu V R; Van Dyke D L; Jackson C E
Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(8):2525-8.
1984: Mu Y; Van Dyke D L; Weiss L; Olgac S
De novo direct tandem duplication of the proximal long arm of chromosome 2: 46,XX,dir dup(2)(q11 X 2q14 X 2).
Journal of medical genetics 1984;21(1):57-8.
1984: Flejter W L; Van Dyke D L; Weiss L
Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.
American journal of human genetics 1984;36(1):218-26.
1984: Van Dyke D L; Babu V R; Jackson C E
Chromosomes in multiple endocrine neoplasia type 2 syndromes.
Henry Ford Hospital medical journal 1984;32(4):266-8.
1983: Talpos G B; Jackson C E; Yott J B; Van Dyke D L
Phenotype mapping of the multiple endocrine neoplasia type II syndrome.
Surgery 1983;94(4):650-4.
1983: Van Dyke D L; Miller M J; Weiss L
The origin of inverted tandem duplications, and phenotypic effects of tandem duplication of the X chromosome long arm.
American journal of medical genetics 1983;15(3):441-50.
1983: Van Dyke D L; Weiss L; Roberson J R; Babu V R
The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age.
American journal of human genetics 1983;35(2):301-8.
1982: Haseltine F P; Lynch V A; Van Dyke D L; Breg W R; Francke U
H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesis.
American journal of medical genetics 1982;13(2):115-23.
1982: Magenis R E; Webb M J; McKean R S; Tomar D; Allen L J; Kammer H; Van Dyke D L; Lovrien E
Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.
Human genetics 1982;62(3):271-6.
1981: Van Dyke D L; Abraham J P; Maeda K; Weiss L; Poel M
Multiple active X chromosomes in myelofibrosis with myeloid metaplasia.
Cancer genetics and cytogenetics 1981;3(2):137-44.
1981: Melnyk A R; Weiss L; Van Dyke D L; Jarvi P
Malformation syndrome of duplication 12q24.1 leads to qter.
American journal of medical genetics 1981;10(4):357-65.
1981: Lee C Y; Madrazo B L; Van Dyke D L; Smith J
Prenatal diagnosis of fetal cystic hygromas associated with generalized lymphangiectasis.
Henry Ford Hospital medical journal 1981;29(2):93-6.
1981: Van Dyke D L; Fluharty A L; Schafer I A; Shapiro L J; Kihara H; Weiss L
Prenatal diagnosis of Maroteaux-Lamy syndrome.
American journal of medical genetics 1981;8(2):235-42.
1979: Kini K R; Van Dyke D L; Weiss L; Logan M S
Ring chromosome 6: case report and review of literature.
Human genetics 1979;50(2):145-9.
1978: Klugo R; Van Dyke D L; Weiss L
Cytogenic studies of cryptorchid testes.
Urology 1978;11(3):255-6.
1977: Van Dyke D L; Palmer C G; Nance W E; Yu P L
Chromosome polymorphism and twin zygosity.
American journal of human genetics 1977;29(5):431-47.
1977: Pai G S; Leach D C; Weiss L; Wolf C; Van Dyke D L
Thyroid abnormalities in 20 children with Turner syndrome.
The Journal of pediatrics 1977;91(2):267-9.
1977: Van Dyke D L; Weiss L; Logan M; Pai G S
The origin and behavior of two isodicentric bisatellited chromosomes.
American journal of human genetics 1977;29(3):294-300.

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