Genotype-phenotype correlations among BRCA14153delA and 5382insC mutation carriers from Latvia-Reference-Cited by-同舟云学术

Genotype-phenotype correlations among BRCA14153delA and 5382insC mutation carriers from Latvia

Published:2011-10-27 Issue:1 Volume:12 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Plakhins Grigorijs,Irmejs Arvids,Gardovskis Andris,Subatniece Signe,Rozite Santa,Bitina Marianna,Keire Guntars,Purkalne Gunta,Teibe Uldis,Trofimovics Genadijs,Miklasevics Edvins,Gardovskis Janis

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-12-147.pdf

Reference24 articles.

1. Tan DS, Marchiò C, Reis-Filho JS: Hereditary breast cancer: from molecular pathology to tailored therapies. J Clin Pathol. 2008, 61 (10): 1073-1082. 10.1136/jcp.2008.057950.

2. Ramus SJ, Gayther SA: The Contribution of BRCA1 and BRCA2 to Ovarian Cancer. Mol Oncol. 2009, 3 (2): 138-150. 10.1016/j.molonc.2009.02.001.

3. Mavaddat N, Antoniou AC, Easton DF, Garcia-Closas M: Genetic susceptibility to breast cancer. Mol Oncol. 2010, 4 (3): 174-191. 10.1016/j.molonc.2010.04.011.

4. Hohenstein P, Fodde R: Of mice and (wo)men: genotype-phenotype correlations in BRCA1. Hum Mol Genet. 2003, 12 (Spec No 2): R271-7.

5. Wu W, Koike A, Takeshita T, Ohta T: The ubiquitin E3 ligase activity of BRCA1 and its biological functions. Cell Division. 2008, 3: 1-10.1186/1747-1028-3-1.

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5. The molecular detection of germline mutations in BRCA1 and BRCA2 genes in a small group of patients from Romania;Romanian Biotechnological Letters;2020-10-18