Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes.

Faiyaz-Ul-Haque, M; Zaidi, S H E; King, L M; Haque, S; Patel, M; Ahmad, M; Siddique, T; Ahmad, W; Tsui, L-C; Cohn, D H

Faiyaz-Ul-Haque, M; Zaidi, S H E; King, L M; Haque, S; Patel, M; Ahmad, M; Siddique, T; Ahmad, W; Tsui, L-C; Cohn, D H.

Affiliation

Faiyaz-Ul-Haque M; Program in Genetics and Genomic Biology, Hospital for Sick Children, Toronto, Canada. muhammad@genet.sickkids.on.ca

Clin Genet ; 67(1): 93-7, 2005 Jan.

Article in En | MEDLINE | ID: mdl-15617554

Subject(s)

Chromosome Mapping; Chromosomes, Human, X/genetics; Genetic Diseases, X-Linked/genetics; Abnormalities, Multiple/genetics; Base Sequence; Chromosome Mapping/methods; DNA Mutational Analysis; Family Health; Female; Haplotypes; Humans; Male; Pedigree

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Mapping / Chromosomes, Human, X / Genetic Diseases, X-Linked Limits: Female / Humans / Male Language: En Journal: Clin Genet Year: 2005 Document type: Article Affiliation country: Canada

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