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Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status

Background—Familial adenomatous polyposis (FAP) is a clinically well defined hereditary disease caused by germline mutations within the adenomatous polyposis coli (APC) gene. Although several techniques are applied in the mutation analysis of FAP kindreds about 20-50% of cases remain unclear, with n...

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Detaylı Bibliyografya
Asıl Yazarlar: Heinimann, K, Mullhaupt, B, Weber, W, Attenhofer, M, Scott, R, Fried, M, Martinoli, S, Muller, H., Dobbie, Z
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1998
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1727303/
https://ncbi.nlm.nih.gov/pubmed/9824350
Etiketler: Etiketle
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