المؤلفون: Kupka S; Department of Anthropology and Human Genetics, University of Tübingen, Germany. susankupka@yahoo.de, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M

المصدر: Human mutation [Hum Mutat] 2002 Mar; Vol. 19 (3), pp. 308-9.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

مواضيع طبية MeSH: Alanine/*genetics , Genetic Predisposition to Disease/*epidemiology , Glycine/*genetics , Hearing Loss, Sensorineural/*epidemiology , Hearing Loss, Sensorineural/*genetics , Mutation/*genetics , RNA, Ribosomal/*genetics, Adult ; Aged ; Amino Acid Substitution/genetics ; Child ; Child, Preschool ; Female ; Genetic Testing ; Germany/epidemiology ; Humans ; Hungary/epidemiology ; Infant ; Male ; Middle Aged ; Pedigree ; Poland/epidemiology