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A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening

Detalles Bibliográficos
Autores principales:	YUAN, ZHI QIANG, WONG, NORA, FOULKES, WILLIAM D, ALPERT, LESLEY, MANGANARO, FORTUNATO, ANDREUTTI-ZAUGG, CORINNE, IGGO, RICHARD, ANTHONY, KIRA, HSIEH, EUGENE, REDSTON, MARK, PINSKY, LEONARD, TRIFIRO, MARK, GORDON, PHILIP H, LASKO, DANA
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 1999
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622028/ https://www.ncbi.nlm.nih.gov/pubmed/10528862 http://dx.doi.org/10.1136/jmg.36.10.792

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