BRCA1 and BRCA2 families in Finland:: haplotype and phenotype analysis and predominance of founder mutations.

被引:0
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作者
Sarantaus, L
Huusko, P
Eerola, H
Launonen, V
Vehmanen, P
Rapakko, K
Gillanders, E
Syrjäkoski, K
Kainu, T
Vahteristo, P
Pääkkönen, K
Hartikainen, J
Blomqvist, C
Löppönen, T
Holli, K
Mannermaa, A
Kere, J
Kallioniemi, OP
Winqvist, R
Nevanlinna, H
机构
[1] Univ Helsinki, Ctr Hosp, Dept Obstet Gynecol & Oncol, Helsinki, Finland
[2] Univ Oulu Hosp, Dept Clin Genet, Oulu, Finland
[3] Tampere Univ, Canc Genet Lab, FIN-33101 Tampere, Finland
[4] NHGRI, Canc Genet Branch, NIH, Bethesda, MD USA
[5] Univ Helsinki, Dept Med Genet, Helsinki, Finland
[6] Univ Helsinki, Finnish Genome Ctr, Helsinki, Finland
[7] Kuopio Univ Hosp, Dept Gynecol, Clin Genet Unit, SF-70210 Kuopio, Finland
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中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
1802
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页码:A320 / A320
页数:1
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