✦ LIBER ✦

Mutation analysis of the BRCA2 gene in 49 site–specific breast cancer families

✍ Scribed by Phelan, Catherine M.; Lancaster, Johnathan M.; Tonin, Patricia; Gumbs, Curtis; Cochran, Charles; Carter, Ron; Ghadirian, Parviz; Perret, Chantal; Moslehi, Roxana; Dion, France

Book ID: 109916003
Publisher: Nature Publishing Group
Year: 1996
Tongue: English
Weight: 435 KB
Volume: 13
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng0596-120

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Erratum: Mutation analysis of the BRCA2

Erratum: Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families

📂 Article 📅 1996 🏛 Nature Publishing Group 🌐 English ⚖ 96 KB

Mutation analysis in the BRCA1 gene in C

Mutation analysis in the BRCA1 gene in Chinese breast cancer families

✍ Wu Zhengyan; Zhen Linlin; Fan Ping 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 274 KB

Mutation analysis in the BRCA2 gene in p

Mutation analysis in the BRCA2 gene in primary breast cancers

✍ Miki, Yoshio; Katagiri, Toyomasa; Kasumi, Fujio; Yoshimoto, Takamasa; Nakamura, 📂 Article 📅 1996 🏛 Nature Publishing Group 🌐 English ⚖ 397 KB

BRCA2 gene mutations in Greek patients w

BRCA2 gene mutations in Greek patients with familial breast cancer

✍ Athanasios Armakolas; Angela Ladopoulou; Irene Konstantopoulou; B. Pararas; Ilia 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 37 KB 👁 2 views

Family history is a well-recognized risk factor for the development of breast cancer. The isolation of BRCA1 and BRCA2 genes, the two major predisposing genes in familial and to early onset breast and ovarian cancer, has resulted to the identification of a large number of families with mutations in

BRCA1 and BRCA2 mutation analysis in bre

BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland

✍ Magdalena Perkowska; Izabela BroŻek; Barbara Wysocka; Karin Haraldsson; Therese 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 66 KB 👁 2 views

Sixty high-risk breast and/or ovarian cancer families from North-Eastern Poland were screened for germline mutations in BRCA1 (MIM# 113705) and BRCA2 (MIM# 600185), using a combination of protein truncation test, denaturing high-performance liquid chromatography and direct sequencing. Sixteen (27%)

New nonsense mutation in the breast canc

New nonsense mutation in the breast cancer-1 gene in a French site-specific breast cancer family

✍ V Laplace-Marieze; N Presneau; C Girodet; V Vidal; C Vaurs; P Rio; Y-J Bignon 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 84 KB 👁 3 views

Duchenne muscular dystrophy (DMD) is an X-linked degenerative disorder of muscle, caused by gross rearrangements by the dystrophin gene in two-thirds of cases. The remaining one-third of patients may carry more subtle mutations that are difficult to detect because of the large size and complexity of