𝔖 Bobbio Scriptorium
✦   LIBER   ✦

An identical novel mutation in BRCA1 and a common haplotype in familial ovarian cancer in non-Ashkenazi Jews

✍ Scribed by Theodor, L; Bar-Sade, R; Kruglikova, A; Ben-Baruch, G; Risel, S; Shiri-Sverdlov, R; Hirsh Yechezkel, G; Modan, B; Papa, MZ; Rechavi, G


Book ID
109837535
Publisher
Nature Publishing Group
Year
1998
Tongue
English
Weight
853 KB
Volume
77
Category
Article
ISSN
0007-0920

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A low frequency of non-founder BRCA1 mut
✍ Catherine M. Phelan; Elaine Kwan; Elaine Jack; Song Li; Cindy Morgan; Jennifer A πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 122 KB πŸ‘ 1 views

The 185delAG and 5382insC founder mutations account for the majority of mutations identified in BRCA1 in Ashkenazi Jewish breast and breast-ovarian cancer families. Few non-founder BRCA1 mutations have been identified to date in these families. We initially screened a panel of 245 Ashkenazi Jewish b

BRCA1 and BRCA2 mutations in Turkish fam
✍ Hulya Yazici; Gordon Glendon; Hilal Yazici; Steve J. Burnie; PΓ‘nar Saip; Faruk B πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 117 KB πŸ‘ 2 views

Ovarian cancer is a clinically important cancer in Turkey. The contribution of BRCA1 and BRCA2 to ovarian cancer in Turkish patients has not previously been described. In this study we investigated the presence of BRCA1 and BRCA2 mutations in 102 consecutively ascertained, hospital-based, ovarian ca