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Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis.
Gong, Y; Krakow, D; Marcelino, J; Wilkin, D; Chitayat, D; Babul-Hirji, R; Hudgins, L; Cremers, C W; Cremers, F P; Brunner, H G; Reinker, K; Rimoin, D L; Cohn, D H; Goodman, F R; Reardon, W; Patton, M; Francomano, C A; Warman, M L.
Affiliation
  • Gong Y; Department of Genetics and Center for Human Genetics, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Ohio, USA.
Nat Genet ; 21(3): 302-4, 1999 Mar.
Article in En | MEDLINE | ID: mdl-10080184
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Collection: 01-internacional Database: MEDLINE Main subject: Synostosis / Abnormalities, Multiple / Proteins / Joints / Mutation Type of study: Prognostic_studies Limits: Adolescent / Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1999 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Synostosis / Abnormalities, Multiple / Proteins / Joints / Mutation Type of study: Prognostic_studies Limits: Adolescent / Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1999 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos