COH1 analysis and linkage study in two Japanese families with Cohen syndrome.

Kondo, I; Shimizu, A; Asakawa, S; Miyamoto, K; Yamagata, H; Tabara, Y; Shimizu, N

Kondo, I; Shimizu, A; Asakawa, S; Miyamoto, K; Yamagata, H; Tabara, Y; Shimizu, N.

Clin Genet ; 67(3): 270-2, 2005 Mar.

Article in En | MEDLINE | ID: mdl-15691367

Subject(s)

Abnormalities, Multiple/genetics; Genetic Linkage; Intellectual Disability/genetics; Membrane Proteins/genetics; Adolescent; Adult; Face/abnormalities; Female; Humans; Japan; Male; Muscle Hypotonia/genetics; Neutropenia/genetics; Pedigree; Phenotype; Syndrome; Vesicular Transport Proteins

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Genetic Linkage / Membrane Proteins / Intellectual Disability Limits: Adolescent / Adult / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Clin Genet Year: 2005 Document type: Article

Search on Google

XML

PubMed Links