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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author 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
author_facet 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
author_sort YUAN, ZHI QIANG
collection PubMed
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spelling pubmed-36220282013-04-15 A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening 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 J Med Genet Letters to the Editor BMJ Publishing Group 1999-10-01 /pmc/articles/PMC3622028/ /pubmed/10528862 http://dx.doi.org/10.1136/jmg.36.10.792 Text en Journal of Medical Genetics
spellingShingle Letters to the Editor
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
A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
title A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
title_full A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
title_fullStr A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
title_full_unstemmed A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
title_short A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
title_sort missense mutation in both hmsh2 andapc in an ashkenazi jewish hnpcc kindred: implications for clinical screening
topic Letters to the Editor
url 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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