Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.

Sugino, S; Fujishita, S; Kamimura, N; Matsumoto, T; Wapenaar, M C; Deng, H X; Shibuya, N; Miike, T; Niikawa, N

Sugino, S; Fujishita, S; Kamimura, N; Matsumoto, T; Wapenaar, M C; Deng, H X; Shibuya, N; Miike, T; Niikawa, N.

Affiliation

Sugino S; Department of Child Development, Kumamoto University School of Medicine, Japan.

Am J Med Genet ; 34(4): 555-61, 1989 Dec.

Article in En | MEDLINE | ID: mdl-2576185

Subject(s)

Chromosome Deletion; Genes; Muscular Dystrophies/genetics; Polymorphism, Restriction Fragment Length; Chromosome Mapping; DNA/genetics; DNA Mutational Analysis; Female; Fetal Diseases/diagnosis; Fetal Diseases/genetics; Genetic Carrier Screening; Humans; Japan; Male; Muscular Dystrophies/diagnosis; Pedigree; Pregnancy; Prenatal Diagnosis; X Chromosome

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Database: MEDLINE Main subject: Polymorphism, Restriction Fragment Length / Chromosome Deletion / Genes / Muscular Dystrophies Type of study: Diagnostic_studies / Guideline Limits: Female / Humans / Male / Pregnancy Country/Region as subject: Asia Language: En Year: 1989 Type: Article

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