Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome.

Ziv, Y; Frydman, M; Lange, E; Zelnik, N; Rotman, G; Julier, C; Jaspers, N G; Dagan, Y; Abeliovicz, D; Dar, H; Borochowitz, Z; Lathrop, M; Gatti, R A; Shiloh, Y

Ziv, Y; Frydman, M; Lange, E; Zelnik, N; Rotman, G; Julier, C; Jaspers, N G; Dagan, Y; Abeliovicz, D; Dar, H; Borochowitz, Z; Lathrop, M; Gatti, R A; Shiloh, Y.

Affiliation

Ziv Y; Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Israel.

Hum Genet ; 88(6): 619-26, 1992 Mar.

Article in En | MEDLINE | ID: mdl-1551665

Subject(s)

Ataxia Telangiectasia/genetics; Genetic Linkage; Ataxia/diagnosis; Ataxia/genetics; Ataxia Telangiectasia/diagnosis; Ataxia Telangiectasia/ethnology; Ataxia Telangiectasia/immunology; Blotting, Southern; Cataract/diagnosis; Cataract/genetics; Cell Line; Child, Preschool; Chromosomes, Human, Pair 11; Consanguinity; DNA/drug effects; DNA/radiation effects; DNA Probes; Diagnosis, Differential; Ethnicity; Female; Genetic Markers; Humans; Infant; Male; Microcephaly/diagnosis; Microcephaly/genetics; Pedigree; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Ataxia Telangiectasia / Genetic Linkage Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans / Infant / Male Language: En Journal: Hum Genet Year: 1992 Document type: Article Affiliation country: Israel Country of publication: Germany

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