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Comments on the origin and size of the worlds Jewish communities
Genetic heterogeneity and homogeneity among the Jewish people
Family history and modes of genetic inheritance
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abnormal acid affected Arabs Ashk Ashkenazi Jewish Ashkenazi Jews associated autosomal dominant autosomal recessive basic defect birth blood cancer carriers cells chromosome Clin Clinical features congenital consanguinity cystic deafness defect The basic deficiency diabetes mellitus diagnosis dwarfism dysplasia dystonia enzyme factor familial dysautonomia females Figure findings G6PD Gaucher disease gene frequency genetic diseases genetic disorders Goodman heterozygotes heterozygous Historical note iminoglycinuria incidence infants inheritance involving Iraq Iraqi Israel Israeli Jewish communities Jewish ethnic groups Jewish families Jewish population Jewry known lesions males malformations mental retardation metabolism Niemann-Pick disease non-Ashkenazi non-Jewish non-Jews normal North Africa observed occur onset Oriental origin parents patients Pediatr pedigree percent plasma prevalence proband Prognosis and treatment References regional enteritis renal Sephardi serum showed sibs skin Source studies symptoms syndrome Table Talmud Tay-Sachs disease therapy tissue torsion dystonia Total Tourette syndrome trait transmission ulcerative colitis Yemenite York