AAAAAA
Results:
1-11
|
Results: 11
Authors:
Vahteristo, P
Syrjakoski, K
Eerola, H
Kainu, T
Holli, K
Blomqvist, C
Kallioniemi, OP
Nevanlinna, H
Citation: P. Vahteristo et al., Re: Population-based study of BRCA1 and BRCA2 mutations in 1035 unselectedFinnish breast cancer patients - Response, J NAT CANC, 93(2), 2001, pp. 153-154
Authors:
Eerola, H
Pukkala, E
Pyrhonen, S
Blomqvist, C
Sankila, R
Nevanlinna, H
Citation: H. Eerola et al., Risk of cancer in BRCA1 and BRCA2 mutation-positive and -negative breast cancer families (Finland), CANC CAUSE, 12(8), 2001, pp. 739-746
Authors:
Eerola, H
Vahteristo, P
Sarantaus, L
Kyyronen, P
Pyrhonen, S
Blomqvist, C
Pukkala, E
Nevanlinna, H
Sankila, R
Citation: H. Eerola et al., Survival of breast cancer patients in BRCA1, BRCA2, and non-BRCA1/2 breastcancer families: A relative survival analysis from Finland, INT J CANC, 93(3), 2001, pp. 368-372
Authors:
Vahteristo, P
Tamminen, A
Karvinen, P
Eerola, H
Eklund, C
Aaltonen, LA
Blomqvist, C
Aittomaki, K
Nevanlinna, H
Citation: P. Vahteristo et al., p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: Further evidence of CHK2 in inherited cancer predisposition, CANCER RES, 61(15), 2001, pp. 5718-5722
Authors:
Vahteristo, P
Eerola, H
Tamminen, A
Blomqvist, C
Nevanlinna, H
Citation: P. Vahteristo et al., A probability model for predicting BRCA1 and BRCA2 mutations in breast andbreast-ovarian cancer families, BR J CANC, 84(5), 2001, pp. 704-708
Authors:
Rapakko, K
Allinen, M
Syrjakoski, K
Vahteristo, P
Huusko, P
Vahakangas, K
Eerola, H
Kainu, T
Kallioniemi, OP
Nevanlinna, H
Winqvist, R
Citation: K. Rapakko et al., Germline TP53 alterations in Finnish breast cancer families are rare and occur at conserved mutation-prone sites, BR J CANC, 84(1), 2001, pp. 116-119
Authors:
Syrjakoski, K
Vahteristo, P
Eerola, H
Tamminen, A
Kivinummi, K
Sarantaus, L
Holli, K
Blomqvist, C
Kallioniemi, OP
Kainu, T
Nevanlinna, H
Citation: K. Syrjakoski et al., Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients, J NAT CANC, 92(18), 2000, pp. 1529-1531
Authors:
Sarantaus, L
Huusko, P
Eerola, H
Launonen, V
Vehmanen, P
Rapakko, K
Gillanders, E
Syrjakoski, K
Kainu, T
Vahteristo, P
Krahe, R
Paakkonen, K
Hartikainen, J
Blomqvist, C
Lopponen, T
Holli, K
Ryynanen, M
Butzow, R
Borg, A
Arver, BW
Holmberg, E
Mannermaa, A
Kere, J
Kallioniemi, OP
Winqvist, R
Nevanlinna, H
Citation: L. Sarantaus et al., Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland, EUR J HUM G, 8(10), 2000, pp. 757-763
Authors:
Eerola, H
Blomqvist, C
Pukkala, E
Pyrhonen, S
Nevanlinna, H
Citation: H. Eerola et al., Familial breast cancer in southern Finland: how prevalent are breast cancer families and can we trust the family history reported by patients?, EUR J CANC, 36(9), 2000, pp. 1143-1148
Authors:
Kainu, T
Juo, SHH
Desper, R
Schaffer, AA
Gillanders, E
Rozenblum, E
Freas-Lutz, D
Weaver, D
Stephan, D
Bailey-Wilson, J
Kallioniemi, OP
Tirkkonen, M
Syrjakoski, K
Kuukasjarvi, T
Koivisto, P
Karhu, R
Holli, K
Arason, A
Johannesdottir, G
Bergthorsson, JT
Johannsdottir, H
Egilsson, V
Barkardottir, RB
Johannsson, O
Haraldsson, K
Sandberg, T
Holmberg, E
Gronberg, H
Olsson, H
Borg, A
Vehmanen, P
Eerola, H
Heikkila, P
Pyrhonen, S
Nevanlinna, H
Citation: T. Kainu et al., Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus, P NAS US, 97(17), 2000, pp. 9603-9608
Authors:
Eerola, H
Blomqvist, C
Pyrhonen, S
Nevanlinna, H
Citation: H. Eerola et al., Familial breast cancer in Southern Finland, DIS MARKER, 15(1-3), 1999, pp. 105-105
Risultati:
1-11
|