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Aliza Amiel
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72
Fejgin, Moshe
34
Gaber, Elena
32
Lishner, Michael
16
Manor, Yosef
9
Sharony, Ram
8
Reish, Orit
8
Kedar, I
8
Kitay-Cohen, Yona
8
Elis, Avishay
8
Yukla, Monayukla
7
Avivi, Lydia
6
Kidron, Dvora
6
Ravid, Mordchai
5
Nagler, Arnon
5
Goldberg-Bittman, Lilach
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All Publications
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2009: Sukenik-Halevy Rivka; Fejgin Moshe; Kidron Devora; Goldberg-Bittman Lilach; Sharony Reuven; Biron-Shental Tal; Kitay-Cohen Yona; Amiel Aliza
Telomere aggregate formation in placenta specimens of pregnancies complicated with pre-eclampsia.
Cancer genetics and cytogenetics 2009;195(1):27-30.
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2009: Hadi Efrat; Sharony Reuven; Goldberg-Bittman Lilach; Biron-Shental Tal; Fejgin Moshe; Amiel Aliza
Telomere aggregates in trisomy 21 amniocytes.
Cancer genetics and cytogenetics 2009;195(1):23-6.
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2009: Goldberg-Bittman Lilach; Amiel Aliza; Hadary Ruth; Fejgin Moshe D; Quitt Miriam; Kitay-Cohen Yona
Telomere capture in hepatitis C infection.
Cancer genetics and cytogenetics 2009;191(2):63-6.
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2008: Kitay-Cohen Y; Goldberg-Bittman L; Hadary R; Fejgin M D; Amiel A
Telomere length in Hepatitis C.
Cancer genetics and cytogenetics 2008;187(1):34-8.
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2008: Goldberg-Bittman Lilach; Kitay-Cohen Yona; Hadari Ruth; Yukla Monayukla; Fejgin Moshe D; Amiel Aliza
Random aneuploidy in chronic hepatitis C patients.
Cancer genetics and cytogenetics 2008;180(1):20-3.
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2007: Sharony Reuven; Amiel Aliza; Einy Reviva; Fejgin Moshe
Prenatal diagnosis of pericentric inversion in homologues of chromosome 9: a decision dilemma.
American journal of perinatology 2007;24(2):137-40.
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2006: Amiel A; Yukla M; Gaber E; Leopold L; Josef G; Fejgin M; Lishner M
Random aneuploidy in CML patients at diagnosis and under imatinib treatment.
Cancer genetics and cytogenetics 2006;168(2):120-3.
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2006: Amiel A; Leopold L; Gronich N; Yukla M; Fejgin M D; Lishner M
The influence of different chromosomal aberrations on molecular cytogenetic parameters in chronic lymphocytic leukemia.
Cancer genetics and cytogenetics 2006;167(2):145-9.
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2006: Biron-Shental Tal; Amiel Aliza; Fejgin Moshe D
Previous aneuploidic offspring in a young woman does not increase the risk for somatic random aneuploidy in subsequent pregnancies.
Acta obstetricia et gynecologica Scandinavica 2006;85(8):1003-7.
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2006: Amiel Aliza; Goldzak Galit; Gaber Elena; Fejgin Moshe D
Molecular cytogenetic characteristics of Down syndrome newborns.
Journal of human genetics 2006;51(6):541-7.
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2005: Amiel A; Goldzak G; Gaber E; Yosef G; Fejgin M D; Yukla M; Lishner M
Random aneuploidy and telomere capture in chronic lymphocytic leukemia and chronic myeloid leukemia patients.
Cancer genetics and cytogenetics 2005;163(1):12-6.
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2005: Amiel A; Gronich N; Yukla M; Suliman S; Josef G; Gaber E; Drori G; Fejgin M D; Lishner M
Random aneuploidy in neoplastic and pre-neoplastic diseases, multiple myeloma, and monoclonal gammopathy.
Cancer genetics and cytogenetics 2005;162(1):78-81.
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2005: Fejgin Moshe D; Pomeranz Meir; Liberman Meytal; Fishman Ami; Amiel Aliza
Fluorescent in situ hybridization: an effective and less costly technique for genetic evaluation of products of conception in pregnancy losses.
Acta obstetricia et gynecologica Scandinavica 2005;84(9):860-3.
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2004: Amiel A; Drori G; Weinstein G; Fejgin M D
Molecular cytogenetic parameters in fibroblasts of ataxia telangiectasia carrier.
Cancer genetics and cytogenetics 2004;153(2):102-7.
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2004: Amiel A; Yukla M; Yogev S; Manor Y; Fejgin M D; Lishner M
Deletion of 5q31 and 7q31 in patients with stable melphalan treated multiple myeloma.
Cancer genetics and cytogenetics 2004;152(1):84-7.
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2004: Amiel A; Peretz G; Slor H; Weinstein G; Fejgin M D
Molecular cytogenetic parameters in fibroblasts from patients and carriers of xeroderma pigmentosum.
Cancer genetics and cytogenetics 2004;149(2):154-60.
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2004: Nagler Arnon; Korenstein-Ilan Avital; Amiel Aliza; Avivi Lydia
Granulocyte colony-stimulating factor generates epigenetic and genetic alterations in lymphocytes of normal volunteer donors of stem cells.
Experimental hematology 2004;32(1):122-30.
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2003: Shohat Mordechai; Frimer Helena; Shohat-Levy Vered; Esmailzadeh Hormoz; Appelman Zvi; Ben-Neriah Ziva; Dar Hanna; Orr-Urtreger Avi; Amiel Aliza; Gershoni Ruth; Manor Esther; Barkai Gad; Shalev Stavit; Gelman-Kohen Zully; Reish Orit; Lev Dorit; Davidov Bella; Goldman Boleslaw
Prenatal diagnosis of Down syndrome: ten year experience in the Israeli population.
American journal of medical genetics. Part A 2003;122A(3):215-22.
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2003: Sharony Reuven; Amiel Aliza; Bouaron Nitsan; Kidron Debora; Itzhaky Dganit; Fejgin Moshe
Congenital deficiency of alpha-fetoprotein and associated chromosomal abnormality in the placenta.
American journal of medical genetics. Part A 2003;121A(2):113-7.
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2003: Sharony Reuven; Drugan Arie; Amiel Aliza; Grinshpun-Cohen Julia; Markov Shlomo; Fejgin Moshe D
Are amniotic fluid alpha-fetoprotein levels influenced by the gender in twin pairs?
Fetal diagnosis and therapy 2003;18(4):281-3.
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2003: Amiel A; Atzmon H; Klein Z; Kidron D; Gaber E; Vassilyev O; Shalom-Paz E; Fishman A; Fejgin M D
Application of comparative genomic hybridization technique for detection of chromosomal aberrations in benign cystic teratoma.
Cancer genetics and cytogenetics 2003;144(1):73-5.
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2003: Amiel A; Biton I; Yukla M; Gaber E; Fejgin M D; Lishner M
The effect of chlorambucil treatment on cytogenetic parameters in chronic lymphocytic leukemia patients.
Cancer genetics and cytogenetics 2003;143(2):113-9.
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2003: Sharony R; Grinshpun-Cohen J; Rabi K; Amiel A; Fejgin M
Low maternal serum concentrations of human chorionic gonadotropin as part of the triple test screening: a follow-up study.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2003;13(5):300-4.
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2003: Amiel A; Kaufman Z; Goldstein E; Bruchim R Bar-Sade; Kidron D; Gaber E; Fejgin M D
Application of comparative genomic hybridization in search for genetic aberrations in fibroadenomas of the breast.
Cancer genetics and cytogenetics 2003;142(2):145-8.
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2003: Reish Orit; Finkelstein Yehuda; Mesterman Ronit; Nachmani Ariela; Wolach Baruch; Fejgin Moshe; Amiel Aliza
Is isolated palatal anomaly an indication to screen for 22q11 region deletion?
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2003;40(2):176-9.
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2003: Amiel A; Ohali A; Fejgin M; Sardos-Albertini F; Bouaron N; Cohen I J; Yaniv I; Zaizov R; Avigad S
Molecular cytogenetic parameters in Ewing sarcoma.
Cancer genetics and cytogenetics 2003;140(2):107-12.
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2002: Korenstein-Ilan Avital; Amiel Aliza; Lalezari Shadan; Lishner Michael; Avivi Lydia
Allele-specific replication associated with aneuploidy in blood cells of patients with hematologic malignancies.
Cancer genetics and cytogenetics 2002;139(2):97-103.
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2002: Reish Orit; Gal Ron; Gaber Elena; Sher Carron; Bistritzer Tzvy; Amiel Aliza
Asynchronous replication of biallelically expressed loci: a new phenomenon in Turner syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics 2002;4(6):439-43.
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2002: Cohen Ninette; Trakhtenbrot Luba; Yukla Mona; Manor Yosef; Gaber Elena; Yosef Gabi; Amariglio Ninette; Rechavi Gideon; Amiel Aliza
SKY detection of chromosome rearrangements in two cases of tMDS with a complex karyotype.
Cancer genetics and cytogenetics 2002;138(2):128-32.
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2002: Amiel Aliza; Reish Orit; Gaber Elena; Masterman Ronit; Tohami Tally; Fejgin Moshe D
Asynchronous replication of alleles in genomes carrying a microdeletion.
The Israel Medical Association journal : IMAJ 2002;4(9):702-5.
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2002: Amiel A; Bouaron N; Kidron D; Sharony R; Gaber E; Fejgin M D
CGH in the detection of confined placental mosaicism (CPM) in placentas of abnormal pregnancies.
Prenatal diagnosis 2002;22(9):752-8.
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2002: Amiel Aliza; Elis Avishay; Maimon Orit; Ellis Martin; Herishano Yair; Gaber Elena; Fejgin Moshe D; Lishner Michael
Replication status in leukocytes of treated and untreated patients with polycythemia vera and essential thrombocytosis.
Cancer genetics and cytogenetics 2002;133(1):34-8.
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2002: Rosen D J D; Kedar I; Amiel A; Ben-Tovim T; Petel Y; Kaneti H; Tohar M; Fejgin M D
A negative second trimester triple test and absence of specific ultrasonographic markers may decrease the need for genetic amniocentesis in advanced maternal age by 60%.
Prenatal diagnosis 2002;22(1):59-63.
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2002: Reish Orit; Lerer Israela; Amiel Aliza; Heyman Eli; Herman Arie; Dolfin Tzipora; Abeliovich Dvorah
Wiedemann-Beckwith syndrome: further prenatal characterization of the condition.
American journal of medical genetics 2002;107(3):209-13.
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2002: Amiel Aliza; Bartoov Benjamin; Pevsner Dina; Sardos-Albertini Federika; Fejgin Moshe D
No intraindividual variation of disomy rate in sperm samples.
Journal of human genetics 2002;47(10):539-42.
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2001: Gurevitch M; Amiel A; Ben-Zion M; Fejgin M; Bartoov B
Acrocentric centromere organization within the chromocenter of the human sperm nucleus.
Molecular reproduction and development 2001;60(4):507-16.
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2001: Kitay-Cohen Y; Amiel A; Ashur Y; Fejgin M D; Herishanu Y; Afanasyev F; Bomstein Y; Lishner M
Analysis of chromosomal aberrations in large hepatocellular carcinomas by comparative genomic hybridization.
Cancer genetics and cytogenetics 2001;131(1):60-4.
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2001: Fejgin M D; Diukman R; Cotton Y; Weinstein G; Amiel A
Fetal cells in the uterine cervix: a source for early non-invasive prenatal diagnosis.
Prenatal diagnosis 2001;21(8):619-21.
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2001: Herishanu Y; Lishner M; Bomstein Y; Kitay-Cohen Y; Fejgin M D; Gaber E; Amiel A
Comparative genomic hybridization in polycythemia vera and essential thrombocytosis patients.
Cancer genetics and cytogenetics 2001;128(2):154-7.
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2001: Amiel A; Elis A; Blumenthal D; Gaber E; Fejgin M D; Dubinsky R; Lishner M
Modified order of allelic replication in lymphoma patients at different disease stages.
Cancer genetics and cytogenetics 2001;125(2):156-60.
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2001: Amiel A; Elis A; Sherker S; Gaber E; Manor Y; Fejgin M D
The influence of cytogenetic aberrations on gene replication in chronic lymphocytic leukemia patients.
Cancer genetics and cytogenetics 2001;125(2):81-6.
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2001: Amiel A; Levi E; Reish O; Sharony R; Fejgin M D
Replication status as a possible marker for genomic instability in cells originating from genotypes with balanced rearrangements.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2001;9(8):611-6.
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2001: Amiel A; Sardos-Albertini F; Fejgin M D; Sharony R; Diukman R; Bartoov B
Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin.
Journal of human genetics 2001;46(5):245-50.
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2000: Kitay-Cohen Y; Amiel A; Hilzenrat N; Buskila D; Ashur Y; Fejgin M; Gaber E; Safadi R; Tur-Kaspa R; Lishner M
Bcl-2 rearrangement in patients with chronic hepatitis C associated with essential mixed cryoglobulinemia type II.
Blood 2000;96(8):2910-2.
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2000: Bruchim I; Kidron D; Amiel A; Altaras M; Fejgin M D
Complete hydatidiform mole and a coexistent viable fetus: report of two cases and review of the literature.
Gynecologic oncology 2000;77(1):197-202.
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2000: Amiel A; Kitay-Cohen Y; Fejgin M D; Lishner M
Replication status as a marker for predisposition for lymphoma in patients with chronic hepatitis C with and without cryoglobulinemia.
Experimental hematology 2000;28(2):156-60.
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2000: Carlebach M; Amiel A; Gaber E; Radnay J; Manor Y; Fejgin M; Lishner M
Multiple myeloma: monoallelic deletions of the tumor suppressor genes TP53 and RB1 in long-term follow-up.
Cancer genetics and cytogenetics 2000;117(1):57-60.
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2000: Amiel A; Reish O; Gaber E; Kedar I; Diukman R; Fejgin M
Replication asynchrony increases in women at risk for aneuploid offspring.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2000;8(2):141-50.
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1999: Amiel A; Fridman K; Elis A; Gaber E; Manor Y; Fejgin M; Lishner M
Deletion 5q31 in patients with stable, melphalan-treated multiple myeloma.
Cancer genetics and cytogenetics 1999;113(1):45-8.
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1999: Amiel A; Mulchanov I; Elis A; Gaber E; Manor Y; Fejgin M; Lishner M
Deletion of 6q27 in chronic lymphocytic leukemia and multiple myeloma detected by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1999;112(1):53-6.
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1999: Amiel A; Korenstein A; Gaber E; Avivi L
Asynchronous replication of alleles in genomes carrying an extra autosome.
European journal of human genetics : EJHG 1999;7(2):223-30.
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1999: Amiel A; Kirgner I; Gaber E; Manor Y; Fejgin M; Lishner M
Replication pattern in cancer: asynchronous replication in multiple myeloma and in monoclonal gammopathy.
Cancer genetics and cytogenetics 1999;108(1):32-7.
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1998: Amiel A; Kolodizner T; Fishman A; Gaber E; Klein Z; Beyth Y; Fejgin M D
Replication pattern of the p53 and 21q22 loci in the premalignant and malignant stages of carcinoma of the cervix.
Cancer 1998;83(9):1966-71.
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1998: Amiel A; Avivi L; Gaber E; Fejgin M D
Asynchronous replication of allelic loci in Down syndrome.
European journal of human genetics : EJHG 1998;6(4):359-64.
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1998: Amiel A; Litmanovitch T; Lishner M; Mor A; Gaber E; Tangi I; Fejgin M; Avivi L
Temporal differences in replication timing of homologous loci in malignant cells derived from CML and lymphoma patients.
Genes, chromosomes & cancer 1998;22(3):225-31.
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1998: Reish O; Wolach B; Amiel A; Kedar I; Dolfin T; Fejgin M
Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
American journal of medical genetics 1998;77(1):72-5.
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1997: Amiel A; Litmanovich T; Gaber E; Lishner M; Avivi L; Fejgin M D
Asynchronous replication of p53 and 21q22 loci in chronic lymphocytic leukemia.
Human genetics 1997;101(2):219-22.
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1997: Fejgin M D; Kedar I; Amiel A; Ben-Tovim T; Chen R; Petel Y; Tepper R
Elevated hCG as an isolated finding during the second trimester biochemical screen: genetic, ultrasonic, and perinatal significance.
Prenatal diagnosis 1997;17(11):1027-31.
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1997: Amiel A; Arbov L; Manor Y; Fejgin M; Elis A; Gaber E; Lishner M
Monoallelic p53 deletion in chronic lymphocytic leukemia detected by interphase cytogenetics.
Cancer genetics and cytogenetics 1997;97(2):97-100.
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1997: Fejgin M D; Arbel-DeRowe Y; Shul N; Amiel A
A false-positive diagnosis of Turner syndrome by amniocentesis.
Prenatal diagnosis 1997;17(1):88-9.
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1996: Amiel A; Elis A; Manor Y; Tangi I; Fejgin M; Lishner M
Fluorescent in situ hybridization (FISH) for the detection of trisomy 8 in acute myeloblastic leukemia.
Leukemia & lymphoma 1996;23(5-6):603-7.
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1996: Elis A; Amiel A; Manor Y; Tangi I; Fejgin M; Lishner M
The detection of trisomies 8 and 9 in patients with essential thrombocytosis by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1996;92(1):14-7.
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1996: Einat M; Nagler A; Amiel A; Fejgin M D; Rudi A; Kashman Y; Fabian I
Synergistic effects of interleukin-11 with other growth factors on the expansion of hematopoietic progenitors from normal individuals and chronic myeloid leukemia patients resistant to treatment with cytosine arabinoside or eilatin.
Leukemia research 1996;20(9):751-9.
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1996: Amiel A; Kidron D; Kedar I; Gaber E; Reish O; Fejgin M D
Are all phenotypically-normal Turner syndrome fetuses mosaics?
Prenatal diagnosis 1996;16(9):791-5.
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1996: Lishner M; Confino-Cohen R; Mekori Y A; Feigin M; Manor Y; Goldberg A; Ravid M; Amiel A
Trisomies 9 and 8 detected by fluorescence in situ hybridization in patients with systemic mastocytosis.
The Journal of allergy and clinical immunology 1996;98(1):199-204.
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1996: Kedar I; Amiel A; Fejgin M; Drugan A
Recurrent anencephaly as a primary manifestation of the acrocallosal syndrome.
American journal of medical genetics 1996;62(4):415-6.
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1996: Fejgin M D; Kidron D; Kedar I; Gaber E; Tepper R; Beyth Y; Amiel A
Genetic diagnosis from formalin-fixed fetal tissue using FISH: a new tool for genetic counseling in subsequent pregnancies.
European journal of obstetrics, gynecology, and reproductive biology 1996;64(2):221-4.
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1995: Lishner M; Lalkin A; Klein A; Yarkoni S; Manor Y; Fejgin M; Leytin V; Ravid M; Amiel A
The BCL-1, BCL-2, and BCL-3 oncogenes are involved in chronic lymphocytic leukemia. Detection by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1995;85(2):118-23.
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1995: Einat M; Lishner M; Amiel A; Nagler A; Yarkorli S; Rudi A; Kashman Y; Markel D; Fabian I
Eilatin: a novel marine alkaloid inhibits in vitro proliferation of progenitor cells in chronic myeloid leukemia patients.
Experimental hematology 1995;23(14):1439-44.
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1995: Shohat M; Akstein E; Davidov B; Barkai G; Legum C; David M; Dar H; Romem Y; Amiel A; Cohen H
Amniocentesis rate and the detection of Down syndrome and other chromosomal anomalies in Israel.
Prenatal diagnosis 1995;15(10):967-70.
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1995: Ishai D; Amiel A; Diukman R; Cogan O; Lichtenstein Z; Abramovici H; Fejgin M D
Uterine cavity lavage: adding FISH to conventional cytogenetics for embryonic sexing and diagnosing common chromosomal aberrations.
Prenatal diagnosis 1995;15(10):961-5.
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1995: Einat M; Nagler A; Lishner M; Amiel A; Yarkoni S; Rudi A; Gellerman G; Kashman Y; Fabian I
Potent antileukemic activity of the novel agents norsegoline and dibezine.
Clinical cancer research : an official journal of the American Association for Cancer Research 1995;1(8):823-9.
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1995: Amiel A; Fejgin M; Appelman Z; Shapiro I; Gaber E; Bachar A; Zamir R; Kedar I; Golbus M
Fluorescent in-situ hybridization (FISH) as an aid to marker chromosome identification in prenatal diagnosis.
European journal of obstetrics, gynecology, and reproductive biology 1995;59(1):103-7.
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1995: Amiel A; Gaber E; Manor Y; Fejgin M; Joseph-Lerner N; Ravid M; Lishner M
Fluorescence in situ hybridization for the detection of trisomies 8 and 9 in polycythemia vera.
Cancer genetics and cytogenetics 1995;79(2):153-6.
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1994: Lishner M; Ravid M; Shapira J; Radnay J; Amiel A; Leytin V; Shapiro C; Klein A
Delta-T-lymphocytosis in a patient with thymoma.
Cancer 1994;74(11):2924-9.
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1994: Davidov B; Goldman B; Akstein E; Barkai G; Legum C; Dar H; Romem Y; Amiel A; Cohen H; Bach G
Prenatal testing for Down syndrome in the Jewish and non-Jewish populations in Israel.
Israel journal of medical sciences 1994;30(8):629-33.
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1994: Amiel A; Lishner M; Lalkin A; Gaber E; Manor Y; Fejgin M; Yarkoni S; Ravid M
Detection of bcl rearrangements in B-CLL by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1994;73(2):165-8.
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1993: Lalkin A; Lishner M; Gaber E; Manor Y; Fejgin M; Ravid M; Amiel A
In situ hybridization: a simple and sensitive method for detection of trisomy 12 in chronic lymphocytic leukemia.
Cancer genetics and cytogenetics 1993;70(1):21-4.
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1993: Joseph-Lerner N; Fejgin M; Ben-Nun I; Legum C; Amiel A
The correlation between the frequency of sister-chromatid exchange and human reproductive hormones.
Mutation research 1993;300(3-4):247-52.
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1993: Fejgin M; Amiel A; Kaneti H; Ben-Nun I; Beyth Y
Fulminant sepsis due to group B beta-hemolytic streptococci following transcervical chorionic villi sampling.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 1993;17(1):142-3.
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1993: Fejgin M D; Amiel A; Kohn G
More about low maternal serum human chorionic gonadotropin and unconjugated estriol values in triploidy.
American journal of obstetrics and gynecology 1993;168(5):1641.
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1993: Amiel A; Yarkoni S; Fejgin M; Gaber E; Nagler A; Manor Y; Lishner M
Clinical detection of BCR-abl fusion by in situ hybridization in chronic myelogenous leukemia.
Cancer genetics and cytogenetics 1993;65(1):32-4.
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1993: Lishner M; Kenet G; Lalkin A; Yarkoni S; Ben-Bassat H; Fejgin M; Rechavi G; Amiel A
Fluorescent in situ hybridization for the detection of t(8:14) in Burkitt's lymphoma.
Acta haematologica 1993;90(4):186-9.
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1992: Fejgin M; Amiel A; Goldberger S; Barnes I; Zer T; Kohn G
Placental insufficiency as a possible cause of low maternal serum human chorionic gonadotropin and low maternal serum unconjugated estriol levels in triploidy.
American journal of obstetrics and gynecology 1992;167(3):766-7.
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1992: Fejgin M; Barnes I; Lipnick N; Magid Z; Kohn G; Amiel A
The dilemma of a low rate of chromosomal mosaicism found in fetal blood sampling.
Prenatal diagnosis 1992;12(2):129-31.
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1992: Barnes I; Amiel A; Fejgin M D
Elevated maternal serum human chorionic gonadotropin in two cases of fetal ventral wall defects.
Prenatal diagnosis 1992;12(1):76-7.
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1991: Zeitune M; Ben-Tovim T; Fejgin M; Amiel A; Beyth Y
Screening for Down's syndrome in older women based on maternal serum alpha-fetoprotein levels and age: preliminary results.
Prenatal diagnosis 1991;11(6):393-8.
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1991: Kohn G; Zamir R; Zer T; Amiel A; Fejgin M
Significance of very low maternal serum human chorionic gonadotropin in prenatal diagnosis of triploidy.
Prenatal diagnosis 1991;11(4):277.
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1990: Fejgin M; Zeitune M; Amiel A; Beyth Y
Elevated maternal serum alpha-fetoprotein level and sex chromosome aneuploidy.
Prenatal diagnosis 1990;10(6):414-6.
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1989: Avivi L; Dotan A; Ravia Y; Amiel A; Shacham H; Neumann Y
Increased spindle resistance to antimicrotubule agents in cells prone to chromosomal nondisjunction.
Human genetics 1989;83(2):165-70.
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1989: Ziv Y; Jaspers N G; Etkin S; Danieli T; Trakhtenbrot L; Amiel A; Ravia Y; Shiloh Y
Cellular and molecular characteristics of an immortalized ataxia-telangiectasia (group AB) cell line.
Cancer research 1989;49(9):2495-501.
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1989: Ziv Y; Amiel A; Jaspers N G; Berkel A I; Shiloh Y
Ataxia-telangiectasia: a variant with altered in vitro phenotype of fibroblast cells.
Mutation research 1989;210(2):211-9.
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