Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel
Toledano-Alhadef, Hagit, Basel-Vanagaite, Lina, Magal, Nurit, Davidov, Bella, Ehrlich, Sophie, Drasinover, Valerie, Taub, Ellen, Halpern, Gabrielle J., Ginott, Nathan, Shohat, Mordechai
Published in American journal of human genetics (01.08.2001)
Published in American journal of human genetics (01.08.2001)
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Journal Article
Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel
BASEL -VANAGAITE, Lina, TAUB, Ellen, HALPERN, Gabrielle J, DRASINOVER, Valerie, MAGAL, Nurit, DAVIDOV, Bella, ZLOTOGORA, Joël, SHOHAT, Mordechai
Published in European journal of human genetics : EJHG (01.02.2007)
Published in European journal of human genetics : EJHG (01.02.2007)
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Journal Article
Prevalence of breast and colorectal cancer in Ashkenazi Jewish carriers of Fanconi anemia and Bloom syndrome
Baris, Hagit N, Kedar, Inbal, Halpern, Gabrielle J, Shohat, Tamy, Magal, Nurit, Ludman, Mark D, Shohat, Mordechai
Published in The Israel Medical Association journal (01.12.2007)
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Published in The Israel Medical Association journal (01.12.2007)
Journal Article
Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis
Mimouni, A, Magal, N, Stoffman, N, Shohat, T, Minasian, A, Krasnov, M, Halpern, G J, Rotter, J I, Fischel-Ghodsian, N, Danon, Y L, Shohat, M
Published in Pediatrics (Evanston) (01.05.2000)
Published in Pediatrics (Evanston) (01.05.2000)
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Identification of the gene causing long QT syndrome in an Israeli family
Tenenbaum, Michal, Lavi, Shahar, Magal, Nurit, Halpern, Gabrielle J, Bolocan, Inbal, Boulos, Monther, Kapeliovich, Michael, Shohat, Mordechai, Hammerman, Haim
Published in The Israel Medical Association journal (01.11.2008)
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Published in The Israel Medical Association journal (01.11.2008)
Journal Article
Differences in infant mortality rates between Jews and Arabs in Israel, 1975-2000
Tarabeia, Jalal, Amitai, Yona, Green, Manfred, Halpern, Gabrielle J, Blau, Sharon, Ifrah, Anneke, Rotem, Naama, Jaber, Lutfi
Published in The Israel Medical Association journal (01.07.2004)
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Published in The Israel Medical Association journal (01.07.2004)
Journal Article
Phenotypic expression of tissue mosaicism in a 45,X/46,X,dicY(q11.2) female
Udler, Y, Kauschansky, A, Yeshaya, J, Freedman, J, Barkai, U, Tobar, A, Okon, E, Halpern, G J, Shohat, M, Legum, C
Published in American journal of medical genetics (01.09.2001)
Published in American journal of medical genetics (01.09.2001)
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Pathological fractures in spondyloenchondrodysplasia : case report
UDLER, Y, HALPERN, G. J, LACHMAN, R. S, RIMOIN, D. L, SHOHAT, M
Published in Pediatric radiology (01.02.2000)
Published in Pediatric radiology (01.02.2000)
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Journal Article
Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel
Basel-Vanagaite, Lina, Taub, Ellen, Halpern, Gabrielle J, Drasinover, Valerie, Magal, Nurit, Davidov, Bella, Zlotogora, Joel, Shohat, Mordechai
Published in European journal of human genetics : EJHG (01.02.2007)
Published in European journal of human genetics : EJHG (01.02.2007)
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Journal Article
Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings
Senecky, Y, Halpern, G J, Inbar, D, Attias, J, Shohat, M
Published in American journal of medical genetics (01.07.2001)
Published in American journal of medical genetics (01.07.2001)
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