BRCA1 mutations: Haplotype and phenotype analysis revisited.

被引:0
|
作者
Szabo, CI
Fleischmann, E
Neuhausen, S
Devilee, P
Goldgar, D
Wagner, T
机构
[1] Int Agcy Res Canc, Unit Genet Epidemiol, Lyon, France
[2] Univ Vienna, Klin Fraunheilkunde, Dept OB GYN, Vienna, Austria
[3] Univ Utah, Salt Lake City, UT USA
[4] Leiden Univ, Med Ctr, Dept Human & Clin Genet, Leiden, Netherlands
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
1832
引用
收藏
页码:A325 / A325
页数:1
相关论文
共 50 条
  • [1] BRCA1 mutations and phenotype
    Grade, K
    Hoffken, K
    Kath, R
    Nothnagel, A
    Bender, E
    Scherneck, S
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1997, 123 (01) : 69 - 70
  • [2] BRCA1 mutations and phenotype
    K. Grade
    K. Höffken
    R. Kath
    A. Nothnagel
    E. Bender
    S. Scherneck
    Journal of Cancer Research and Clinical Oncology, 1997, 123 : 69 - 70
  • [3] BRCA1 and BRCA2 families in Finland:: haplotype and phenotype analysis and predominance of founder mutations.
    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
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A320 - A320
  • [4] Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study
    Neuhausen, SL
    Mazoyer, S
    Friedman, L
    Stratton, M
    Offit, K
    Caligo, A
    Tomlinson, G
    CannonAlbright, L
    Bishop, T
    Kelsell, D
    Solomon, E
    Weber, B
    Couch, F
    Struewing, J
    Tonin, P
    Durocher, F
    Narod, S
    Skolnick, MH
    Lenoir, G
    Serova, O
    Ponder, B
    StoppaLyonnet, D
    Easton, D
    King, MC
    Goldgar, DE
    AMERICAN JOURNAL OF HUMAN GENETICS, 1996, 58 (02) : 271 - 280
  • [5] Haplotype analysis in German families with recurrent BRCA1 and BRCA2 mutations
    B Wappenschmidt
    A Golla
    A Kempe
    A Meindl
    RK Schmutzler
    Breast Cancer Research, 3 (Suppl 1)
  • [6] Mutations at BRCA1:: The medullary breast carcinoma revisited
    Eisinger, F
    Jacquemier, J
    Charpin, C
    Stoppa-Lyonnet, D
    Bressac-de Paillerets, B
    Peyrat, JP
    Longy, M
    Guinebretière, JM
    Sauvan, R
    Noguchi, T
    Birnbaum, D
    Sobol, H
    CANCER RESEARCH, 1998, 58 (08) : 1588 - 1592
  • [7] Brca1 revisited
    不详
    NATURE GENETICS, 1996, 13 (04) : 389 - 389
  • [8] BRCA1 mutations
    DiCioccio, RA
    Werness, BA
    Piver, MS
    GENES CHROMOSOMES & CANCER, 2003, 37 (02): : 222 - 222
  • [9] Discovery of BRCA1/BRCA2 founder variants by haplotype analysis
    Kwon, Won Kyung
    Jang, Hyeok-Jae
    Lee, Jeong Eon
    Park, Yeon Hee
    Ryu, Jai Min
    Yu, Jonghan
    Jang, Ja-Hyun
    Kim, Jong-Won
    CANCER GENETICS, 2022, 266 : 19 - 27
  • [10] A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing
    Dorum, A
    Moller, P
    Kamsteeg, EJ
    Scheffer, H
    Burton, M
    Heimdal, KR
    Mæhle, LO
    Hovig, E
    Tropé, CG
    van der Hout, AH
    van der Meulen, MA
    Buys, CHCM
    Meerman, GJT
    EUROPEAN JOURNAL OF CANCER, 1997, 33 (14) : 2390 - 2392