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Human Mutation|March 29, 2000
The E148Q mutation in the MEFV gene: is it a disease-causing mutation or a sequence variant?E Ben-Chetrit, I Lerer, E Malamud, et al.American Journal of Human Genetics|May 1, 1995
Homozygosity for Waardenburg syndromeJ Zlotogora, I Lerer, S Bar-David, et al.American Journal of Medical Genetics|June 1, 1982
Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15))R Voss, I Lerer, G Maftzir, et al.Human Mutation|April 29, 1999
A large deletion mutation in the CFTR gene (3120+1Kbdel8.6Kb): a founder mutation in the Palestinian Arabs. Mutation in brief no. 231. OnlineI Lerer, A Laufer-Cahana, J R Rivlin, et al.European Journal of Human Genetics : EJHG|January 1, 1995
Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomesD Abeliovich, J Dagan, M Werner, et al.Prenatal Diagnosis|February 1, 1997
Trisomy 2: confined placental mosaicism in a fetus with intrauterine growth retardationI Ariel, I Lerer, S Yagel, et al.Human Mutation|October 23, 2001
A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi JewsI Lerer, M Sagi, Z Ben-Neriah, et al.European Journal of Human Genetics : EJHG|February 5, 1998
Transient neonatal diabetes mellitus in a child with invdup(6)(q22q23) of paternal originE I Arthur, J Zlotogora, I Lerer, et al.American Journal of Medical Genetics|December 2, 1996
t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspringD Abeliovich, J Dagan, I Lerer, et al.American Journal of Medical Genetics|November 14, 2000
Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delTI Lerer, M Sagi, E Malamud, et al.Pageof 5