المؤلفون: Vallada, H., Craddock, N., Vasques, L., Curtis, D., Kirov, G., Lauriano, V., Gentil, V., Passos-Bueno, R., Murray, R. M., Zatz, M.

المصدر: Journal of Affective Disorders; 1996, Vol. 41 Issue: 3 p217-221, 5p

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المؤلفون: Bashir R; Department of Human Genetics, University of Newcastle upon Tyne, NE2 4AA, United Kingdom., Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K

المصدر: Genomics [Genomics] 1996 Apr 01; Vol. 33 (1), pp. 46-52.

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

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 8800135 Publication Model: Print Cited Medium: Print ISSN: 0888-7543 (Print) Linking ISSN: 08887543 NLM ISO Abbreviation: Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 2*, Muscular Dystrophies/*genetics, Animals ; Base Sequence ; Chromosome Mapping ; Chromosomes, Artificial, Yeast ; DNA Primers ; Female ; Genetic Linkage ; Genetic Markers ; Haplotypes ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Mice ; Molecular Sequence Data ; Pedigree