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Items: 1 to 20 of 35

1.

Mutation nomenclature: nicknames, systematic names, and unique identifiers.

Beutler E, McKusick VA, Motulsky AG, Scriver CR, Hutchinson F.

Hum Mutat. 1996;8(3):203-6. No abstract available.

PMID:
8889577
2.

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations.

Caligo MA, Ghimenti C, Cipollini G, Ricci S, Brunetti I, Marchetti V, Olsen R, Neuhausen S, Shattuck-Eidens D, Conte PF, Skolnick MH, Bevilacqua G.

Oncogene. 1996 Oct 3;13(7):1483-8.

PMID:
8875986
3.

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2.

Peelen T, Cornelis RS, van Vliet M, Petrij-Bosch A, Cleton-Jansen AM, Meijers-Heijboer H, Klijn JG, Vasen HF, Cornelisse CJ, Devilee P.

Eur J Hum Genet. 1996;4(4):225-30.

PMID:
8875189
4.

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2.

Roa BB, Boyd AA, Volcik K, Richards CS.

Nat Genet. 1996 Oct;14(2):185-7.

PMID:
8841191
6.

A common BRCA1 mutation in Norwegian breast and ovarian cancer families?

Andersen TI, Børresen AL, Møller P.

Am J Hum Genet. 1996 Aug;59(2):486-7. No abstract available.

7.

Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds.

Berman DB, Wagner-Costalas J, Schultz DC, Lynch HT, Daly M, Godwin AK.

Am J Hum Genet. 1996 Jun;58(6):1166-76.

8.

Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden.

Johannsson O, Ostermeyer EA, Håkansson S, Friedman LS, Johansson U, Sellberg G, Brøndum-Nielsen K, Sele V, Olsson H, King MC, Borg A.

Am J Hum Genet. 1996 Mar;58(3):441-50.

9.

New Austrian mutation in BRCA1 gene detected in three unrelated HBOC families.

Wagner TM, Möslinger R, Zielinski C, Scheiner O, Breiteneder H.

Lancet. 1996 May 4;347(9010):1263. No abstract available.

PMID:
8622478
10.

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE.

Am J Hum Genet. 1996 Feb;58(2):271-80.

11.

A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.

Serova O, Montagna M, Torchard D, Narod SA, Tonin P, Sylla B, Lynch HT, Feunteun J, Lenoir GM.

Am J Hum Genet. 1996 Jan;58(1):42-51.

12.
13.

Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families.

Friedman LS, Szabo CI, Ostermeyer EA, Dowd P, Butler L, Park T, Lee MK, Goode EL, Rowell SE, King MC.

Am J Hum Genet. 1995 Dec;57(6):1284-97.

14.
15.

Mutation of human short tandem repeats.

Weber JL, Wong C.

Hum Mol Genet. 1993 Aug;2(8):1123-8.

PMID:
8401493
16.

High-density genetic map of the BRCA1 region of chromosome 17q12-q21.

Anderson LA, Friedman L, Osborne-Lawrence S, Lynch E, Weissenbach J, Bowcock A, King MC.

Genomics. 1993 Sep;17(3):618-23.

PMID:
8244378
17.

Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test.

van der Luijt R, Khan PM, Vasen H, van Leeuwen C, Tops C, Roest P, den Dunnen J, Fodde R.

Genomics. 1994 Mar 1;20(1):1-4.

PMID:
8020934
18.

Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE.

Lancet. 1994 Mar 19;343(8899):692-5.

PMID:
7907678
19.

Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families.

Friedman LS, Ostermeyer EA, Szabo CI, Dowd P, Lynch ED, Rowell SE, King MC.

Nat Genet. 1994 Dec;8(4):399-404.

PMID:
7894493
20.

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families.

Simard J, Tonin P, Durocher F, Morgan K, Rommens J, Gingras S, Samson C, Leblanc JF, Bélanger C, Dion F, et al.

Nat Genet. 1994 Dec;8(4):392-8.

PMID:
7894492

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