The entire coding regions of BRCA1 and BRCA2 were screened for mutations by heteroduplex analysis in 51 Mexican breast cancer patients. One BRCA1 and one BRCA2 truncating mutation each was identified in the group of 32 (6%) early-onset breast cancer patients (< or =35 years). Besides these two likel
โฆ LIBER โฆ
The Role of MMAC1 Mutations in Early-Onset Breast Cancer: Causative in Association with Cowden Syndrome and Excluded in BRCA1-Negative Cases
โ Scribed by Hui C. Tsou; David H.-F. Teng; Xiao Li Ping; Valeria Brancolini; Thaylon Davis; Rong Hu; Xiao Xun Xie; Alexandra C. Gruener; Carolina A. Schrager; Angela M. Christiano; Charis Eng; Peter Steck; Jurg Ott; Sean V. Tavtigian; Monica Peacocke
- Book ID
- 117852208
- Publisher
- American Society of Human Genetics
- Year
- 1997
- Tongue
- English
- Weight
- 843 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/301607
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
BRCA1 and BRCA2 mutation analysis of ear
โ
Pablo Ruiz-Flores; Olga M. Sinilnikova; Michael Badzioch; A.L. Calderon-Garcidue
๐
Article
๐
2002
๐
John Wiley and Sons
๐
English
โ 50 KB
๐ 2 views
Mutations in the BRCA1 gene in families
โ
Castilla, Lucio H.; Couch, Fergus J.; Erdos, Michael R.; Hoskins, Kent F.; Calzo
๐
Article
๐
1994
๐
Nature Publishing Group
๐
English
โ 681 KB
Mutation analysis of BRIP1/BACH1 in BRCA
โ
A-Yong Cao; Juan Huang; Zhen Hu; Wen-Feng Li; Zhong-Liang Ma; Li-Li Tang; Bin Zh
๐
Article
๐
2008
๐
Springer US
๐
English
โ 189 KB
BRCA1, BRCA2 and TP53 mutations in very
BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives
โ
Fiona Lalloo; Jennifer Varley; Anthony Moran; David Ellis; Lindsay OโDair; Paul
๐
Article
๐
2006
๐
Elsevier Science
๐
English
โ 143 KB
BRCA1 and BRCA2 mutations in women with
โ
Lenka Foretova; Eva Machackova; Marie Navratilova; Hana Pavlu; Marcela Hruba; Mi
๐
Article
๐
2004
๐
John Wiley and Sons
๐
English
โ 45 KB
๐ 2 views
Germline mutations in BRCA1 and BRCA2 account for majority of hereditary breast and ovarian cancer. The complete coding sequence analysis of both genes was carried out in 197 breast/ovarian cancer patients from high-risk families and 53 patients with sporadic breast/ovarian cancer. In summary, 59 mu
The prevalence of PALB2 germline mutatio
โ
A-Yong Cao; Juan Huang; Zhen Hu; Wen-Feng Li; Zhong-Liang Ma; Li-Li Tang; Bin Zh
๐
Article
๐
2008
๐
Springer US
๐
English
โ 217 KB