Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome predisposing to tumors of the parathyroid, endocrine pancreas, anterior pituitary, adrenal glands, and diffuse neuroendocrine tissues. The MEN1 gene has been assigned, by linkage analysis and loss of heterozygosity, to chro...

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Detalhes bibliográficos
Main Authors: Giraud, S, Zhang, C X, Serova-Sinilnikova, O, Wautot, V, Salandre, J, Buisson, N, Waterlot, C, Bauters, C, Porchet, N, Aubert, J P, Emy, P, Cadiot, G, Delemer, B, Chabre, O, Niccoli, P, Leprat, F, Duron, F, Emperauger, B, Cougard, P, Goudet, P, Sarfati, E, Riou, J P, Guichard, S, Rodier, M, Meyrier, A, Caron, P, Vantyghem, M C, Assayag, M, Peix, J L, Pugeat, M, Rohmer, V, Vallotton, M, Lenoir, G, Gaudray, P, Proye, C, Conte-Devolx, B, Chanson, P, Shugart, Y Y, Goldgar, D, Murat, A, Calender, A
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377295/
https://ncbi.nlm.nih.gov/pubmed/9683585
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