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Volumn 42, Issue 6, 2005, Pages 511-513

Sex ratio skewing of offspring in families with hereditary susceptibility to breast cancer

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; CANCER SUSCEPTIBILITY; FAMILIAL CANCER; FAMILY STUDY; FEMALE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; ONCOGENE; OVARY CANCER; PRIORITY JOURNAL; PROGENY; SEX DIFFERENTIATION; SEX RATIO; X CHROMOSOME INACTIVATION;

EID: 20544476613     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2004.027722     Document Type: Article
Times cited : (5)

References (17)
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  • 3
    • 0036727705 scopus 로고    scopus 로고
    • Homozygous Tsix mutant mice reveal a sex-ratio distortion and revert to random X-inactivation
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    • Lee, J.T.1
  • 4
    • 0033577046 scopus 로고    scopus 로고
    • Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer
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    • (1999) J Natl Cancer Inst , vol.91 , pp. 339-346
    • Buller, R.E.1    Sood, A.K.2    Lallas, T.3    Buekers, T.4    Skilling, J.S.5
  • 5
    • 0043198132 scopus 로고    scopus 로고
    • Association between BRCA1 mutations and ratio of female to male births in offspring of families with breast cancer, ovarian cancer, or both
    • de la Hoya M, Fernandez JM, Tosar A, Godino J, Sanchez de Abajo A, Vidart JA, Perez-Segura P, Diaz-Rubio E, Caldes T. Association between BRCA1 mutations and ratio of female to male births in offspring of families with breast cancer, ovarian cancer, or both. JAMA 2003;290:929-31.
    • (2003) JAMA , vol.290 , pp. 929-931
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  • 12
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    • Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing
    • Unger MA, Nathanson KL, Calzone K, Antin-Ozerkis D, Shih HA, Martin AM, Lenoir GM, Mazoyer S, Weber BL. Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing. Am J Hum Genet 2000;67:841-50.
    • (2000) Am J Hum Genet , vol.67 , pp. 841-850
    • Unger, M.A.1    Nathanson, K.L.2    Calzone, K.3    Antin-Ozerkis, D.4    Shih, H.A.5    Martin, A.M.6    Lenoir, G.M.7    Mazoyer, S.8    Weber, B.L.9
  • 14
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    • Cancer incidence in BRCA1 mutation carriers
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.