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Items: 5

1.

Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management.

Lynch HT, Casey MJ, Snyder CL, Bewtra C, Lynch JF, Butts M, Godwin AK.

Mol Oncol. 2009 Apr;3(2):97-137. doi: 10.1016/j.molonc.2009.02.004. Review.

2.

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T, Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel JN, Gordon PH, MacNamara E, King MC, Hampel H, De La Chapelle A, Boyd J, Offit K, Rennert G, Chong G, Ellis NA.

Am J Hum Genet. 2002 Dec;71(6):1395-412.

3.

The genetic basis of Muir-Torre syndrome includes the hMLH1 locus.

Bapat B, Xia L, Madlensky L, Mitri A, Tonin P, Narod SA, Gallinger S.

Am J Hum Genet. 1996 Sep;59(3):736-9. No abstract available.

4.

Evidence for genetic anticipation in non-Mendelian diseases.

Paterson AD, Kennedy JL, Petronis A.

Am J Hum Genet. 1996 Jul;59(1):264-8. No abstract available.

5.

Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

Froggatt NJ, Koch J, Davies R, Evans DG, Clamp A, Quarrell OW, Weissenbach J, Hodgson SV, Ponder BA, Barton DE, et al.

J Med Genet. 1995 May;32(5):352-7.

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