Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.

Brzustowicz, L M; Mérette, C; Kleyn, P W; Lehner, T; Castilla, L H; Penchaszadeh, G K; Das, K; Munsat, T L; Ott, J; Gilliam, T C

Brzustowicz, L M; Mérette, C; Kleyn, P W; Lehner, T; Castilla, L H; Penchaszadeh, G K; Das, K; Munsat, T L; Ott, J; Gilliam, T C.

Affiliation

Brzustowicz LM; Department of Psychiatry, Columbia University, College of Physicians and Surgeons, New York, NY 10032.

Hum Hered ; 43(6): 380-7, 1993.

Article in En | MEDLINE | ID: mdl-7904586

Subject(s)

Chromosomes, Human, Pair 5; Muscular Atrophy, Spinal/genetics; Adolescent; Alleles; Child; Child, Preschool; Chromosome Mapping; Chronic Disease; DNA, Satellite/analysis; Female; Genetic Linkage; Genetic Variation; Genotype; Humans; Lod Score; Male; Muscular Atrophy, Spinal/classification; Odds Ratio; Pedigree; Polymorphism, Restriction Fragment Length; Retrospective Studies

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 5 / Muscular Atrophy, Spinal Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Hum Hered Year: 1993 Document type: Article

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