-
1
-
-
33646570913
-
A genome wide linkage search for breast cancer susceptibility genes
-
Smith P, McGuffog L, Easton DF et al (2006) A genome wide linkage search for breast cancer susceptibility genes. Genes Chromosomes Cancer 45:646-655
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 646-655
-
-
Smith, P.1
McGuffog, L.2
Easton, D.F.3
-
2
-
-
0027467494
-
Extracolonic cancer in hereditary nonpolyposis colorectal cancer
-
Watson P, Lynch HT (1993) Extracolonic cancer in hereditary nonpolyposis colorectal cancer. Cancer 71:677-85
-
(1993)
Cancer
, vol.71
, pp. 677-85
-
-
Watson, P.1
Lynch, H.T.2
-
3
-
-
0029585997
-
Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome
-
Aarno M, Mcklin JP, Aaltonen LA et al (1995) Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome. Int J Cancer 64:430-433
-
(1995)
Int J Cancer
, vol.64
, pp. 430-433
-
-
Aarno, M.1
McKlin, J.P.2
Aaltonen, L.A.3
-
4
-
-
0029966487
-
Molecular genetic evidence of the occurrence of breast cancer as an integral tumour in patients with the hereditary non-polyposis colorectal carcinoma syndrome
-
Risinger JI, Barrett JC, Watson P et al (1996) Molecular genetic evidence of the occurrence of breast cancer as an integral tumour in patients with the hereditary non-polyposis colorectal carcinoma syndrome. Cancer 77:1836-1843
-
(1996)
Cancer
, vol.77
, pp. 1836-1843
-
-
Risinger, J.I.1
Barrett, J.C.2
Watson, P.3
-
5
-
-
0034956758
-
Molecular Pathologic analysis enhances the diagnosis and management of Muir-Torre syndrome and gives insight into its underlying molecular pathogenesis
-
Southey MC, Young MA, Whitty J et al (2001) Molecular Pathologic analysis enhances the diagnosis and management of Muir-Torre syndrome and gives insight into its underlying molecular pathogenesis. Am J Surg Path 25:936-941
-
(2001)
Am J Surg Path
, vol.25
, pp. 936-941
-
-
Southey, M.C.1
Young, M.A.2
Whitty, J.3
-
6
-
-
0036173948
-
Exclusion of breast cancer as an integral tumour of hereditary nonpolyposi colorectal cancer
-
Muller A, Edmonston TB, Corao DA et al (2002) Exclusion of breast cancer as an integral tumour of hereditary nonpolyposi colorectal cancer. Cancer Res 62:1012-1019
-
(2002)
Cancer Res
, vol.62
, pp. 1012-1019
-
-
Muller, A.1
Edmonston, T.B.2
Corao, D.A.3
-
7
-
-
0037373830
-
Correspondence re Muller et al. exclusion of breast cancer as an integral tumour of hereditary nonpolyposi colorectal cancer
-
de Leeuw WJ, Puijenbroek M, Tollenaar RAEM et al (2003) Correspondence re Muller et al. exclusion of breast cancer as an integral tumour of hereditary nonpolyposi colorectal cancer. Cancer Res 63:1148-1149
-
(2003)
Cancer Res
, vol.63
, pp. 1148-1149
-
-
De Leeuw, W.J.1
Puijenbroek, M.2
Tollenaar, R.A.E.M.3
-
8
-
-
0035162347
-
Hereditary nonpolyposis colorectal cancer in 95 families: Differences and similarities between mutation-positive and mutation-negative kindreds
-
Scott RJ, McPhillips M, Meldrum CJ et al (2001) Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds. Am J Hum Genet 68:118-127
-
(2001)
Am J Hum Genet
, vol.68
, pp. 118-127
-
-
Scott, R.J.1
McPhillips, M.2
Meldrum, C.J.3
-
9
-
-
0034989895
-
Is breast cancer part of the tumour spectrum of hereditary nonpolyposis colorectal cancer?
-
Vasen HFA, Morreau H, Nortier JWR (2001) Is breast cancer part of the tumour spectrum of hereditary nonpolyposis colorectal cancer? Am J Hum Genet 68:1533-1534
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1533-1534
-
-
Vasen, H.F.A.1
Morreau, H.2
Nortier, J.W.R.3
-
10
-
-
45749118523
-
-
Accessed Sept 2007
-
http://www.kconfab.org. Accessed Sept 2007
-
-
-
-
11
-
-
0033287525
-
Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS)
-
Hopper JL, Chenevix-Trench G, Jolley DJ et al (1999) Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS). J Natl Cancer Inst Monogr 26:95-100
-
(1999)
J Natl Cancer Inst Monogr
, vol.26
, pp. 95-100
-
-
Hopper, J.L.1
Chenevix-Trench, G.2
Jolley, D.J.3
-
12
-
-
0028289691
-
Background rational and protocol for a case-control-family study of breast cancer
-
Hopper JL, Giles GG, McCredie MR, Boyle P (1994) Background rational and protocol for a case-control-family study of breast cancer. Breast 3:79-86
-
(1994)
Breast
, vol.3
, pp. 79-86
-
-
Hopper, J.L.1
Giles, G.G.2
McCredie, M.R.3
Boyle, P.4
-
14
-
-
45749102231
-
Strong familial risks associated with early-onset breast cancer are only partially BRCA1- or BRCA2-related
-
448-457, 2003
-
Dite GS, Jenkins MA, Hocking JS et al (2002) Strong familial risks associated with early-onset breast cancer are only partially BRCA1- or BRCA2-related. JNCI 19:95,448-457, 2003
-
(2002)
JNCI
, vol.19
, pp. 95
-
-
Dite, G.S.1
Jenkins, M.A.2
Hocking, J.S.3
-
15
-
-
0037028740
-
Dominant negative ATM mutations in breast cancer families
-
Erratum in: J Natl Cancer Inst 2002 94, 952
-
Chenevix-Trench G, Spurdle AB, Gatei M et al (2002) Dominant negative ATM mutations in breast cancer families. J Natl Cancer Inst 94, 205-215. Erratum in: J Natl Cancer Inst 2002 94, 952
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 205-215
-
-
Chenevix-Trench, G.1
Spurdle, A.B.2
Gatei, M.3
-
16
-
-
33847682259
-
BRCA1 promoter deletions in young women with breast cancer and a strong family history: A population-based study
-
Smith LD, Tesoriero AA, Ramus SJ et al (2007) BRCA1 promoter deletions in young women with breast cancer and a strong family history: a population-based study. Eur J Cancer 43:823-827
-
(2007)
Eur J Cancer
, vol.43
, pp. 823-827
-
-
Smith, L.D.1
Tesoriero, A.A.2
Ramus, S.J.3
-
17
-
-
33644949696
-
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
-
Epub 2006 Feb 13
-
Mann GJ, Thorne H, Belleine RL et al (2006) Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource. Breast Cancer Res 8(1):R12. Epub 2006 Feb 13
-
(2006)
Breast Cancer Res
, vol.8
, Issue.1
-
-
Mann, G.J.1
Thorne, H.2
Belleine, R.L.3
-
18
-
-
26644441586
-
Mismatch repair gene mutation testing, immunohistochemistry and microsatellite instability testing in a population-based series of unselected early-onset colorectal cancers
-
Southey MC, Jenkins MA, Mead L et al (2005) Mismatch repair gene mutation testing, immunohistochemistry and microsatellite instability testing in a population-based series of unselected early-onset colorectal cancers. J Clin Oncol 23:6524-6532
-
(2005)
J Clin Oncol
, vol.23
, pp. 6524-6532
-
-
Southey, M.C.1
Jenkins, M.A.2
Mead, L.3
-
19
-
-
33747141723
-
Genomic rearrangements in hMSH2 and hMLH1 in early-onset colorectal cancer: A population-based study
-
Smith L, Tesoriero A, Mead L et al (2006) Genomic rearrangements in hMSH2 and hMLH1 in early-onset colorectal cancer: a population-based study. Clin Genet 70:250-252
-
(2006)
Clin Genet
, vol.70
, pp. 250-252
-
-
Smith, L.1
Tesoriero, A.2
Mead, L.3
-
20
-
-
33644529562
-
Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer families
-
Tesoriero AA, Wong EM, Jenkins MA et al (2005) Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer families. Hum Mutat 26:495
-
(2005)
Hum Mutat
, vol.26
, pp. 495
-
-
Tesoriero, A.A.1
Wong, E.M.2
Jenkins, M.A.3
-
21
-
-
45749151904
-
-
Accessed Sept 2006
-
http://www.violin.genet.sickkids.on.ca/~ali/splicesitefinder.html. Accessed Sept 2006
-
-
-
-
22
-
-
0030768854
-
Hereditary nonpolyposis colorectal cancer (HNPCC): Eight novel germline mutations in hMSH2 or hMLH1 genes
-
Wehner M, Buschhausen L, Lamberti C et al (1997) Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes. Hum Mutat 10:241-244
-
(1997)
Hum Mutat
, vol.10
, pp. 241-244
-
-
Wehner, M.1
Buschhausen, L.2
Lamberti, C.3
-
23
-
-
0028955451
-
Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis
-
Wijnen J, Vasen H, Khan PM et al (1995) Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. Am J Hum Genet 56:1060-1066
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1060-1066
-
-
Wijnen, J.1
Vasen, H.2
Khan, P.M.3
|