Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 9

1.

Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.

Jenkins MA, Baglietto L, Dowty JG, Van Vliet CM, Smith L, Mead LJ, Macrae FA, St John DJ, Jass JR, Giles GG, Hopper JL, Southey MC.

Clin Gastroenterol Hepatol. 2006 Apr;4(4):489-98.

PMID:
16616355
2.

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review.

Mitchell RJ, Farrington SM, Dunlop MG, Campbell H.

Am J Epidemiol. 2002 Nov 15;156(10):885-902. Review.

PMID:
12419761
3.
4.

Anticipating phenotypic differences from genetic mutations.

You YN.

Dis Colon Rectum. 2015 Jan;58(1):143-4. doi: 10.1097/DCR.0000000000000271. Review. No abstract available.

PMID:
25489706
5.

Mismatch repair gene deficiency and genetic anticipation in Lynch syndrome: myth or reality?

Ponti G, Ruini C, Tomasi A.

Dis Colon Rectum. 2015 Jan;58(1):141-2. doi: 10.1097/DCR.0000000000000275. Review. No abstract available.

PMID:
25489705
6.

Establishing a clinical and molecular diagnosis for hereditary colorectal cancer syndromes: Present tense, future perfect?

Jansen M, Menko FH, Brosens LA, Giardiello FM, Offerhaus GJ.

Gastrointest Endosc. 2014 Dec;80(6):1145-55. doi: 10.1016/j.gie.2014.07.049. Review. No abstract available.

PMID:
25434663
7.
8.

PMS2 monoallelic mutation carriers: the known unknown.

Goodenberger ML, Thomas BC, Riegert-Johnson D, Boland CR, Plon SE, Clendenning M, Win AK, Senter L, Lipkin SM, Stadler ZK, Macrae FA, Lynch HT, Weitzel JN, de la Chapelle A, Syngal S, Lynch P, Parry S, Jenkins MA, Gallinger S, Holter S, Aronson M, Newcomb PA, Burnett T, Le Marchand L, Pichurin P, Hampel H, Terdiman JP, Lu KH, Thibodeau S, Lindor NM.

Genet Med. 2016 Jan;18(1):13-9. doi: 10.1038/gim.2015.27. Epub 2015 Apr 9. Review.

9.

Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes.

Lindor NM, Hopper J, Dowty J.

Fam Cancer. 2016 Jul;15(3):367-70. doi: 10.1007/s10689-016-9896-2. Review.

Supplemental Content

Support Center