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European Journal of Human Genetics : EJHG|January 1, 1995
Medical genetics in IsraelJ Zlotogora, J Chemke
Journal of Medical Genetics|December 1, 1995
Familial café au lait spots: a variant of neurofibromatosis type 1D Abeliovich, Z Gelman-Kohan, S Silverstein, et al.
Journal De Genetique Humaine|December 1, 1976
Familial macroglossia-omphalocele syndromeJ Chemke
Israel Journal of Medical Sciences|March 1, 1986
Prenatal diagnosis of genetic diseasesJ Chemke
American Journal of Medical Genetics|January 1, 1994
High frequencies of human genetic diseases: founder effect with genetic drift or selection?J Zlotogora
American Journal of Medical Genetics|October 15, 1994
On the inheritance of the split hand/split foot malformationJ Zlotogora
American Journal of Medical Genetics|December 8, 1998
Selection for carriers of recessive diseases: a common phenomenon?J Zlotogora
American Journal of Medical Genetics|March 13, 1995
Major gene is responsible for anencephaly among Iranian JewsJ Zlotogora
American Journal of Medical Genetics|December 15, 1991
Problems in diagnosis and delineation of inherited disorders in highly inbred populationsJ Zlotogora
American Journal of Medical Genetics|April 15, 1993
Mutations in von Recklinghausen neurofibromatosis: an hypothesisJ Zlotogora
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