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

Détails

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Etat: Public
Version: Final published version
Licence: Non spécifiée
ID Serval
serval:BIB_12097
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
UNIL/CHUV
Titre
A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening.
Périodique
Journal of Medical Genetics
Auteur⸱e⸱s
Yuan Z.Q., Wong N., Foulkes W.D., Alpert L., Manganaro F., Andreutti-Zaugg C., Iggo R., Anthony K., Hsieh E., Redston M., Pinsky L., Trifiro M., Gordon P.H., Lasko D.
ISSN
0022-2593
Statut éditorial
Publié
Date de publication
1999
Volume
36
Numéro
10
Pages
790-793
Langue
anglais
Notes
Publication types: Letter ; Research Support, Non-U.S. Gov't Publication Status: ppublish
Mots-clé
Adaptor Proteins, Signal Transducing, Adenomatous Polyposis Coli Protein, Carrier Proteins, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Cytoskeletal Proteins/genetics, DNA-Binding Proteins, Female, Genetic Predisposition to Disease, Humans, Jews, Male, Microsatellite Repeats, MutS Homolog 2 Protein, Mutation, Missense, Neoplasm Proteins/genetics, Nuclear Proteins, Nucleic Acid Conformation, Nucleic Acid Hybridization, Pedigree, Proto-Oncogene Proteins/genetics, Risk Factors
URN
urn:nbn:ch:serval-BIB_120972
OAI-PMH
oai:serval.unil.ch:BIB_12097
Pubmed
10528862
Web of science
000083038400014
Création de la notice
19/11/2007 13:02
Dernière modification de la notice
20/08/2019 13:39
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