BRCA1 mutations in family members with breast cancer history

被引：0
|
作者：
Xhetani, Merita [1 ,2 ]
Hasa, Albina [3 ]
Laze, Blerta [4 ]
机构：
[1] Univ Tirana, Dept Biol, Fac Nat Sci, Tirana, Albania
[2] Univ Tirana, Ctr Mol Diagnost & Genet Res, Fac Nat Sci, Tirana, Albania
[3] Univ Tirana, Dept Biol, Fac Nat Sci, Tirana, Albania
[4] Univ Vlora Ismail Qemali, Dept Biol, Vlora, Albania
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
EP01.030
引用
收藏
页码：913 / 913
页数：1
相关论文
共 50 条
  • [21] Effect of BRCA1 and BRCA2 on the association between breast cancer risk and family history
    Claus, EB
    Schildkraut, J
    Iversen, ES
    Berry, D
    Parmigiani, G
    JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (23) : 1824 - 1829
  • [22] Association of polymorphisms with a family history of cancer and the presence of germline mutations in the BRCA1/BRCA2 genes
    Gabriela C. Fernandes
    Rodrigo A. D. Michelli
    Cristovam Scapulatempo-Neto
    Edenir I. Palmero
    Hereditary Cancer in Clinical Practice, 14
  • [23] Association of polymorphisms with a family history of cancer and the presence of germline mutations in the BRCA1/BRCA2 genes
    Fernandes, Gabriela C.
    Michelli, Rodrigo A. D.
    Scapulatempo-Neto, Cristovam
    Palmero, Edenir I.
    HEREDITARY CANCER IN CLINICAL PRACTICE, 2016, 14
  • [24] Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations
    Ane Y. Steffensen
    Lars Jønson
    Bent Ejlertsen
    Anne-Marie Gerdes
    Finn C. Nielsen
    Thomas V. O. Hansen
    Familial Cancer, 2010, 9 : 283 - 287
  • [25] Sequence analysis of BRCA1 and BRCA2:: Correlation of mutations with family history and ovarian cancer risk
    Frank, TS
    Manley, SA
    Olopade, OI
    Cummings, S
    Garber, JE
    Bernhardt, B
    Antman, K
    Russo, D
    Wood, ME
    Mullineau, L
    Isaacs, C
    Peshkin, B
    Buys, S
    Venne, V
    Rowley, PT
    Loader, S
    Offit, K
    Robson, M
    Hampel, H
    Brener, D
    Winer, EP
    Clark, S
    Weber, B
    Strong, LC
    Rieger, P
    McClure, M
    Ward, BE
    Shattuck-Eidens, D
    Oliphant, A
    Skolnick, MH
    Thomas, A
    JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (07) : 2417 - 2425
  • [26] Analysis of BRCA1 and BRCA2 mutations in an Iranian family with hereditary breast and ovarian cancer syndrome
    Moslehi, R
    Kariminejad, MH
    Ghaffari, V
    Narod, S
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 117A (03) : 304 - 305
  • [27] A breast cancer family from Spain with germline mutations in both the BRCA1 and BRCA2 genes
    Caldes, T.
    de la Hoya, M.
    Tosar, A.
    Sulleiro, S.
    Godino, J.
    Ibanez, D.
    Martin, M.
    Perez-Segura, P.
    Diaz-Rubio, E.
    JOURNAL OF MEDICAL GENETICS, 2002, 39 (08)
  • [28] Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations
    Steffensen, Ane Y.
    Jonson, Lars
    Ejlertsen, Bent
    Gerdes, Anne-Marie
    Nielsen, Finn C.
    Hansen, Thomas V. O.
    FAMILIAL CANCER, 2010, 9 (03) : 283 - 287
  • [29] Family history, BRCA mutations and breast cancer in Vietnamese women
    Ginsburg, O. M.
    Dinh, N. V.
    To, T. V.
    Quang, L. H.
    Linh, N. D.
    Duong, B. T. H.
    Royer, R.
    Llacuachaqui, M.
    Tulman, A.
    Vichodez, G.
    Li, S.
    Love, R. R.
    Narod, S. A.
    CLINICAL GENETICS, 2011, 80 (01) : 89 - 92
  • [30] Founder BRCA1 and BRCA2 mutations in early-onset French Canadian breast cancer cases unselected for family history
    Tonin, PN
    Perret, C
    Lambert, JA
    Paradis, AJ
    Kantemiroff, T
    Benoît, MH
    Martin, G
    Foulkes, WD
    Ghadirian, P
    INTERNATIONAL JOURNAL OF CANCER, 2001, 95 (03) : 189 - 193
12345