๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families

โœ Scribed by Ford, D. (author);Easton, D. F. (author);Stratton, M. (author);Narod, S. (author);Goldgar, D. (author);Devilee, P. (author);Bishop, D. T. (author);Weber, B. (author);Lenoir, G. (author);Chang-Claude, J. (author);Sobol, H. (author);Teare, M. D. (author);Struewing, J. (author);Arason, A. (author);Scherneck, S. (author);Peto, J. (author);Rebbeck, T. R. (author);Tonin, P. (author);Neuhausen, S. (author);Barkardottir, R. (author);Eyfjord, J. (author);Lynch, H. (author);Ponder, B. A.J. (author);Gayther, S. A. (author);Birch, J. M. (author);Lindblom, A. (author);Stoppa-Lyonnet, D. (author);Bignon, Y. (author);Borg, A. (author);Hamann, U. (author);Haites, N. (author);Scott, R. J. (author);Maugard, C. M. (author);Vasen, H. (author);Seitz, S. (author);Cannon-Albright, L. A. (author);Schofield, A. (author);Zelada-Hedman, M. (author)


Book ID
117852320
Publisher
Cell Press
Year
1998
Tongue
English
Weight
141 KB
Volume
62
Category
Article
ISSN
0002-9297

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


BRCA1 and BRCA2 mutations in Russian fam
โœ Irina V. Tereschenko; Victoria M. Basham; Bruce A.J. Ponder; Paul D.P. Pharoah ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 24 KB ๐Ÿ‘ 2 views

We have screened index cases from 25 Russian breast/ovarian cancer families for germ-line mutations in all coding exons of the BRCA1 and BRCA2 genes, using multiplex heteroduplex analysis. In addition we tested 22 patients with breast cancer diagnosed before age 40 without family history and 6 patie

Novel germline mutations in the BRCA1 an
โœ Mani T. Valarmathi; Meenakshi Sawhney; Suryanarayana S. V. Deo; Nootan K. Shukla ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 97 KB ๐Ÿ‘ 2 views

The two major hereditary breast/ovarian cancer predisposition tumor suppressor genes, BRCA1 and BRCA2 that perform apparently generic cellular functions nonetheless cause tissue-specific syndromes in the human population when they are altered, or mutated in the germline. However, little is known abo

BRCA1 and BRCA2 sequence variants in Chi
โœ Xiangcheng Zhi; Csilla Szabo; Sandrine Chopin; Nicola Suter; Qing-Sheng Wang; El ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 41 KB ๐Ÿ‘ 2 views

A series of 45 high-risk breast cancer patients, consisting of 25 affected individuals from 16 families in China with at least two cases of breast cancer and 20 cases of breast cancer diagnosed under age 35 without reported family history, were studied for germline mutations of the BRCA1 and BRCA2 g