✦ LIBER ✦

Corrigendum: BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

Book ID: 109918963
Publisher: Nature Publishing Group
Year: 1997
Tongue: English
Weight: 53 KB
Volume: 17
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1297-503a

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

BRCA1 genomic deletions are major founde

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

✍ Petrij-Bosch, Anne; Peelen, Tamara; van Vliet, Margreethe; Eijk, Ronald van; Olm 📂 Article 📅 1997 🏛 Nature Publishing Group 🌐 English ⚖ 658 KB

Non-founder BRCA1 mutations in Russian b

Non-founder BRCA1 mutations in Russian breast cancer patients

✍ Aglaya G. Iyevleva; Evgeny N. Suspitsin; Karin Kroeze; Tatiana V. Gorodnova; Ann 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 323 KB

BRCA1 and BRCA2 founder mutations in pat

BRCA1 and BRCA2 founder mutations in patients with bilateral breast cancer

✍ Gershoni-Baruch, Ruth; Dagan, Efrat; Fried, Getta; Kepten, Ilana; Robinson, Elie 📂 Article 📅 1999 🏛 Nature Publishing Group 🌐 English ⚖ 134 KB

Founder BRCA1/2 Mutations among Male Pat

Founder BRCA1/2 Mutations among Male Patients with Breast Cancer in Israel

✍ Jeffery P. Struewing; Zakia M. Coriaty; Elaine Ron; Alejandro Livoff; Mirian Kon 📂 Article 📅 1999 🏛 American Society of Human Genetics 🌐 English ⚖ 55 KB

Strong founder effects in BRCA1 mutation

Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia

✍ Bela Csokay; Laima Tihomirova; Aivars Stengrevics; Olga Sinicka; Edith Olah 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 31 KB

Germ-line mutations of the BRCA1 gene account for approximately half of the cases of hereditary breast/ovarian cancers. We have screened index patients from 15 breast cancer families and 8 sporadic breast cancer patients from Latvia for mutations in all coding exons of the BRCA1 gene, using combined

Founder mutation in the BRCA1 gene in Ma

Founder mutation in the BRCA1 gene in Malay breast cancer patients from Singapore

✍ Ann S.G. Lee; G.H. Ho; P.C. Oh; C. Balram; L.L. Ooi; D.T.H. Lim; C.Y. Wong; G.S. 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 48 KB 👁 1 views

The mutation spectrum of the BRCA1 gene among ethnic groups from Asia has not been well studied. We investigated the frequency of mutations in the BRCA1 gene among Malay breast cancer patients from Singapore, independent of family history. By using the protein truncation test (PTT) and direct sequen