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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 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.Clinical and Experimental Rheumatology|October 10, 2002
Molecular diagnosis of FMF: lessons from a study of 446 unrelated individualsE Ben-Chetrit, S Urieli-Shoval, S Calko, et al.American Journal of Human Genetics|November 21, 2000
The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish populationS Silverstein, I Lerer, K Buiting, et al.American Journal of Medical Genetics|August 1, 1994
Molecular diagnosis of Prader-Willi syndrome: parent-of-origin dependent methylation sites and non-isotopic detection of (CA)n dinucleotide repeat polymorphismsI Lerer, V Meiner, I Pashut-Lavon, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Myotonic dystrophy: molecular analysis of Israeli patientsD Abeliovich, I Lerer, I Pashut-Lavon, et al.Journal of Medical Genetics|February 1, 1992
Cystic fibrosis mutations delta F508 and G542X in Jewish patientsI Lerer, M Sagi, G R Cutting, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Machado-Joseph disease: correlation between the clinical features, the CAG repeat length and homozygosity for the mutationI Lerer, D Merims, D Abeliovich, et al.American Journal of Human Genetics|May 1, 1995
Homozygosity for Waardenburg syndromeJ Zlotogora, I Lerer, S Bar-David, 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.Pageof 40