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Results: 1 to 20 of 87

1.

Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindreds.

Peltomäki P, Sistonen P, Mecklin JP, Pylkkänen L, Järvinen H, Simons JW, Cho KR, Vogelstein B, de la Chapelle A.

Cancer Res. 1991 Aug 15;51(16):4135-40.

PMID:
1868434
[PubMed - indexed for MEDLINE]
Free Article
2.

Hereditary nonpolyposis colon cancer: analysis of linkage to 2p15-16 places the COCA1 locus telomeric to D2S123 and reveals genetic heterogeneity in seven Canadian families.

Green RC, Narod SA, Morasse J, Young TL, Cox J, Fitzgerald GW, Tonin P, Ginsburg O, Miller S, Jothy S, et al.

Am J Hum Genet. 1994 Jun;54(6):1067-77.

PMID:
8198129
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.

Nyström-Lahti M, Parsons R, Sistonen P, Pylkkänen L, Aaltonen LA, Leach FS, Hamilton SR, Watson P, Bronson E, Fusaro R, et al.

Am J Hum Genet. 1994 Oct;55(4):659-65.

PMID:
7942843
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.

Peltomäki P, Sistonen P, Mecklin JP, Pylkkänen L, Aaltonen L, Nordling S, Kere J, Järvinen H, Hamilton SR, Petersen G, et al.

Cancer Res. 1992 Aug 15;52(16):4530-3.

PMID:
1643645
[PubMed - indexed for MEDLINE]
Free Article
5.

Chromosome 2p linkage analysis in hereditary non-polyposis colon cancer.

Kohonen-Corish MR, Doe WF, St John DJ, Macrae FA.

J Gastroenterol Hepatol. 1995 Jan-Feb;10(1):76-80.

PMID:
7620112
[PubMed - indexed for MEDLINE]
6.

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.

Nyström-Lahti M, Sistonen P, Mecklin JP, Pylkkänen L, Aaltonen LA, Järvinen H, Weissenbach J, de la Chapelle A, Peltomäki P.

Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6054-8.

PMID:
8016114
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

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.

PMID:
7616541
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma.

Liu SR, Zhao B, Wang ZJ, Wan YL, Huang YT.

World J Gastroenterol. 2004 Sep 15;10(18):2647-51.

PMID:
15309712
[PubMed - indexed for MEDLINE]
Free Article
9.

Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity.

Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San-Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH.

J Bone Miner Res. 1998 Jun;13(6):911-7.

PMID:
9626621
[PubMed - indexed for MEDLINE]
10.

Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer.

Lindblom A, Tannergård P, Werelius B, Nordenskjöld M.

Nat Genet. 1993 Nov;5(3):279-82.

PMID:
7903889
[PubMed - indexed for MEDLINE]
11.

Linkage studies with 17q and 18q markers in a breast/ovarian cancer family.

Milner BJ, Allan LA, Kelly KF, Cruickshank D, Hall M, Johnston A, Kitchener H, Parkin D, Haites N.

Am J Hum Genet. 1993 Apr;52(4):761-6.

PMID:
8096360
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Recurrent deletions at 6q in early age of onset non-HNPCC- and non-FAP-associated intestinal carcinomas. Evidence for a novel cancer susceptibility locus at 6q14-q22.

Bläker H, Mechtersheimer G, Sutter C, Hertkorn C, Kern MA, Rieker RJ, Penzel R, Schirmacher P, Kloor M.

Genes Chromosomes Cancer. 2008 Feb;47(2):159-64.

PMID:
18008368
[PubMed - indexed for MEDLINE]
13.

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.

Easton DF, Bishop DT, Ford D, Crockford GP.

Am J Hum Genet. 1993 Apr;52(4):678-701.

PMID:
8460634
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.

Thomas HJ, Whitelaw SC, Cottrell SE, Murday VA, Tomlinson IP, Markie D, Jones T, Bishop DT, Hodgson SV, Sheer D, Northover JM, Talbot IC, Solomon E, Bodmer WF.

Am J Hum Genet. 1996 Apr;58(4):770-6.

PMID:
8644741
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.

Orenstein SR, Shalaby TM, Finch R, Pfuetzer RH, DeVandry S, Chensny LJ, Bannada MM, Whitcomb DC.

Am J Gastroenterol. 2002 Nov;97(11):2725-32.

PMID:
12425539
[PubMed - indexed for MEDLINE]
16.

Genetic mapping of a locus predisposing to human colorectal cancer.

Peltomäki P, Aaltonen LA, Sistonen P, Pylkkänen L, Mecklin JP, Järvinen H, Green JS, Jass JR, Weber JL, Leach FS, et al.

Science. 1993 May 7;260(5109):810-2.

PMID:
8484120
[PubMed - indexed for MEDLINE]
17.

Tumour spectrum in hereditary non-polyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC". A population-based study in northern Italy. Colorectal Cancer Study Group.

Benatti P, Sassatelli R, Roncucci L, Pedroni M, Fante R, Di Gregorio C, Losi L, Gelmini R, Ponz de Leon M.

Int J Cancer. 1993 May 28;54(3):371-7.

PMID:
8509211
[PubMed - indexed for MEDLINE]
18.

Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome.

Risinger JI, Barrett JC, Watson P, Lynch HT, Boyd J.

Cancer. 1996 May 1;77(9):1836-43.

PMID:
8646682
[PubMed - indexed for MEDLINE]
19.

Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.

Mineharu Y, Inoue K, Inoue S, Yamada S, Nozaki K, Hashimoto N, Koizumi A.

Stroke. 2007 Apr;38(4):1174-8. Epub 2007 Feb 22.

PMID:
17322081
[PubMed - indexed for MEDLINE]
Free Article
20.

Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families.

Johnson V, Lipton LR, Cummings C, Eftekhar Sadat AT, Izatt L, Hodgson SV, Talbot IC, Thomas HJ, Silver AJ, Tomlinson IP.

J Med Genet. 2005 Oct;42(10):756-62. Epub 2005 Mar 23.

PMID:
15788729
[PubMed - indexed for MEDLINE]
Free PMC Article

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