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Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta.

Autosomal dominant osteogenesis imperfecta (OI) is a heterogeneous group of disorders. Molecular haplotypes associated with the pro alpha 2(I) gene of human type I procollagen were used for genetic linkage studies in a group of 10 families with OI. The clinical phenotypes of the families studied wer...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Falk, C T, Schwartz, R C, Ramirez, F, Tsipouras, P
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1986
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684781/
https://ncbi.nlm.nih.gov/pubmed/3006479
Etiketak: Etiketa erantsi
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