-
1
-
-
34247542087
-
CHEK2 1100delC is present in familial breast cancer cases of the Basque Country
-
doi: 10.1007/s10549-006-9351-4
-
Martínez-Bouzas C, Beristain E, Guerra I et al (2007) CHEK2 1100delC is present in familial breast cancer cases of the Basque Country. Breast Cancer Res Treat, doi: 10.1007/s10549-006-9351-4
-
(2007)
Breast Cancer Res Treat
-
-
Martínez-Bouzas, C.1
Beristain, E.2
Guerra, I.3
-
2
-
-
18544389716
-
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
Meijers-Heijboer H, van den Ouweland A, Klijn J et al (2002) Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 31:55-59
-
(2002)
Nat Genet
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
Van Den Ouweland, A.2
Klijn, J.3
-
3
-
-
34250315627
-
Increased risk of breast cancer associated with CHEK2*1100delC
-
Weischer M, Bojesen SE, Tybjaerg-Hansen A et al (2007) Increased risk of breast cancer associated with CHEK2*1100delC. J Clin Oncol 25:57-63
-
(2007)
J Clin Oncol
, vol.25
, pp. 57-63
-
-
Weischer, M.1
Bojesen, S.E.2
Tybjaerg-Hansen, A.3
-
4
-
-
18444379055
-
A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer
-
Vahteristo P, Bartkova J, Eerola H et al (2002) A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet 71:432-438
-
(2002)
Am J Hum Genet
, vol.71
, pp. 432-438
-
-
Vahteristo, P.1
Bartkova, J.2
Eerola, H.3
-
5
-
-
34547735957
-
Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation
-
Schmidt MK, Tollenaar RA, de Kemp SR et al (2007) Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2*1100delC germline mutation. J Clin Oncol 25:64-69
-
(2007)
J Clin Oncol
, vol.25
, pp. 64-69
-
-
Schmidt, M.K.1
Tollenaar, R.A.2
De Kemp, S.R.3
-
6
-
-
33846012859
-
A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers
-
Thompson D, Seal S, Schutte M et al (2006) A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers. Cancer Epidemiol Biomarkers Prev 15:2542-2545
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 2542-2545
-
-
Thompson, D.1
Seal, S.2
Schutte, M.3
-
7
-
-
3042582651
-
CHEK2*1100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
-
CHEK2 Breast Cancer Case-Control Consortium
-
CHEK2 Breast Cancer Case-Control Consortium (2004) CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet 74:1175-1182
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1175-1182
-
-
-
8
-
-
21644484444
-
Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women
-
Friedrichsen DM, Malone KE, Doody DR et al (2004) Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women. Breast Cancer Res 6:R629-R635
-
(2004)
Breast Cancer Res
, vol.6
-
-
Friedrichsen, D.M.1
Malone, K.E.2
Doody, D.R.3
-
9
-
-
33749039966
-
The CHEK2 gene and inherited breast cancer susceptibility
-
Nevanlinna H, Bartek J (2006) The CHEK2 gene and inherited breast cancer susceptibility. Oncogene 25:5912-5919
-
(2006)
Oncogene
, vol.25
, pp. 5912-5919
-
-
Nevanlinna, H.1
Bartek, J.2
-
10
-
-
0344825130
-
The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population
-
Osorio A, Rodríguez-López R, Diez O et al (2004) The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population. Int J Cancer 108:54-56
-
(2004)
Int J Cancer
, vol.108
, pp. 54-56
-
-
Osorio, A.1
Rodríguez-López, R.2
Diez, O.3
-
11
-
-
23244435517
-
Absence of CHEK2 mutations in Spanish families with hereditary breast cancer
-
Bellosillo B, Tusquests I, Longaron R et al (2005) Absence of CHEK2 mutations in Spanish families with hereditary breast cancer. Cancer Genet Cytogenet 161:93-95
-
(2005)
Cancer Genet Cytogenet
, vol.161
, pp. 93-95
-
-
Bellosillo, B.1
Tusquests, I.2
Longaron, R.3
-
12
-
-
21244439203
-
The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families
-
Sanchez de Abajo A, de la Hoya M, Godino J et al (2005) The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families. Fam Cancer 4:183-186
-
(2005)
Fam Cancer
, vol.4
, pp. 183-186
-
-
De Sanchez Abajo, A.1
De La Hoya, M.2
Godino, J.3
-
13
-
-
34247490187
-
Screening for large rearrangements of the BRCA2 gene in n Spanish breast/ovarian cancer families
-
doi: 10.1007/s10549-006-9376-8
-
Gutiérrez-Enríquez S, Díez O, de la Hoya M et al (2007) Screening for large rearrangements of the BRCA2 gene in n Spanish breast/ovarian cancer families. Breast Cancer Res Treat, doi: 10.1007/s10549-006-9376-8
-
(2007)
Breast Cancer Res Treat
-
-
Gutiérrez-Enríquez, S.1
Díez, O.2
De La Hoya, M.3
|