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Links from PubMed

Items: 8

1.

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO.

Evans DG, Eccles DM, Rahman N, Young K, Bulman M, Amir E, Shenton A, Howell A, Lalloo F.

J Med Genet. 2004 Jun;41(6):474-80.

2.

Management updates for women with a BRCA1 or BRCA2 mutation.

Nusbaum R, Isaacs C.

Mol Diagn Ther. 2007;11(3):133-44. Review.

PMID:
17570734
3.

Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review.

Gerhardus A, Schleberger H, Schlegelberger B, Gadzicki D.

Eur J Hum Genet. 2007 Jun;15(6):619-27. Epub 2007 Mar 7. Review.

4.

BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk families.

Sinilnikova OM, Mazoyer S, Bonnardel C, Lynch HT, Narod SA, Lenoir GM.

Fam Cancer. 2006;5(1):15-20. Review.

PMID:
16528604
5.

Development of a scoring system to screen for BRCA1/2 mutations.

Evans GR, Lalloo F.

Methods Mol Biol. 2010;653:237-47. doi: 10.1007/978-1-60761-759-4_14. Review.

PMID:
20721747
6.

BRCA1 and BRCA2: the genetic testing and the current management options for mutation carriers.

Palma M, Ristori E, Ricevuto E, Giannini G, Gulino A.

Crit Rev Oncol Hematol. 2006 Jan;57(1):1-23. Epub 2005 Dec 6. Review.

PMID:
16337408
7.

[Prospects for genetic diagnosis].

Shimoji T, Miki Y.

Nihon Rinsho. 2007 Jun 28;65 Suppl 6:241-4. Review. Japanese. No abstract available.

PMID:
17682161
8.

Recent Enhancements to the Genetic Risk Prediction Model BRCAPRO.

Mazzola E, Blackford A, Parmigiani G, Biswas S.

Cancer Inform. 2015 May 10;14(Suppl 2):147-57. doi: 10.4137/CIN.S17292. eCollection 2015. Review.

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