Caricamento...

Germline PTEN mutations in Cowden syndrome-like families.

Cowden syndrome (CS) or multiple hamartoma syndrome (MIM 158350) is an autosomal dominant disorder with an increased risk for breast and thyroid carcinoma. The diagnosis of CS, as operationally defined by the International Cowden Consortium, is made when a patient, or family, has a combination of pa...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Marsh, D J, Dahia, P L, Caron, S, Kum, J B, Frayling, I M, Tomlinson, I P, Hughes, K S, Eeles, R A, Hodgson, S V, Murday, V A, Houlston, R, Eng, C
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1998
Soggetti:
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051477/
https://ncbi.nlm.nih.gov/pubmed/9832031
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !