Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataract.

Carter, J M; McLean, W H; West, S; Quinlan, R A

Carter, J M; McLean, W H; West, S; Quinlan, R A.

Affiliation

Carter JM; Department of Biochemistry, University of Dundee, Dundee, DD1 5EH, United Kingdom.

Biochem Biophys Res Commun ; 270(2): 432-6, 2000 Apr 13.

Article in En | MEDLINE | ID: mdl-10753642

Subject(s)

Cataract/genetics; Chromosomes, Human, Pair 3; Eye Proteins/genetics; Genes, Dominant; Genetic Linkage; Intermediate Filament Proteins/genetics; Polymorphism, Genetic; Base Sequence; Cataract/congenital; Chromosome Mapping; DNA Primers; Genetic Markers; Humans; Male; Microsatellite Repeats/genetics; Pedigree

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Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Cataract / Chromosomes, Human, Pair 3 / Eye Proteins / Genes, Dominant / Intermediate Filament Proteins / Genetic Linkage Type of study: Diagnostic_studies Limits: Humans / Male Language: En Journal: Biochem Biophys Res Commun Year: 2000 Document type: Article Affiliation country: United kingdom Country of publication: United States

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