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Human Heredity|January 1, 1982
Digital dermatoglyphics of the SamaritansB Bonne-Tamir, D F Roberts, E CoopeEuropean Journal of Human Genetics : EJHG|July 6, 2000
Deafness heterogeneity in a Druze isolate from the Middle East: novel OTOF and PDS mutations, low prevalence of GJB2 35delG mutation and indication for a new DFNB locusA Adato, L Raskin, C Petit, et al.Fertility and Sterility|May 1, 1986
Male fertility in factor XIII deficiencyM Frydman, B Bonne-Tamir, E Braude, et al.Journal of Andrology|May 1, 1991
Assessment of the hypothalamic-pituitary-testicular function in male patients with Wilson's diseaseM Frydman, A Kauschansky, B Bonne-Tamir, et al.Clinical Genetics|April 1, 1979
Genetic studies in a family with inverted nipples (mammillae invertita)R Shafir, B Bonne-Tamir, S Ashbel, et al.Journal of Forensic Sciences|September 16, 1999
Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groupsA Amar, C Brautbar, U Motro, et al.Israel Journal of Medical Sciences|May 1, 1991
Genetic affinities of Ethiopian JewsA Zoossmann-Diskin, A Ticher, I Hakim, et al.Human Immunology|August 10, 1999
Molecular analysis of HLA class II polymorphisms among different ethnic groups in IsraelA Amar, O J Kwon, U Motro, et al.American Journal of Human Genetics|October 23, 1997
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse originsA Adato, D Weil, H Kalinski, et al.Journal of Medical Genetics|May 1, 1997
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle diseaseS Iyengar, H Kalinsky, S Weiss, et al.Pageof 3