BRCA1/2 missense mutations and the value of in-silico analyses-Reference-Cited by-同舟云学术

BRCA1/2 missense mutations and the value of in-silico analyses

Published:2017-11 Issue:11 Volume:60 Page:572-577
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Sadowski Carolin E.,Kohlstedt Daniela,Meisel Cornelia,Keller Katja,Becker Kerstin,Mackenroth Luisa,Rump Andreas,Schröck Evelin,Wimberger Pauline,Kast Karin

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference38 articles.

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3. A 24-color metaphase-based radiation assay discriminates heterozygous BRCA2 mutation carriers from controls by chromosomal radiosensitivity;Becker;Breast cancer Res. Treat.,2012

4. Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases;Caputo;Nucleic acids Res.,2012

5. Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR);Chan;Hum. Mutat.,2007

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