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Volumn 94, Issue 3, 2010, Pages 1097.e5-1097.e8

Molecular cytogenetic definition of a translocation t(X;15) associated with premature ovarian failure

Author keywords

Array CGH; chromosome aberration; FISH; infertility; lymphocytic karyotype; premature ovarian failure; X autosome translocations

Indexed keywords

ESTROGEN; FOLLITROPIN; LUTEINIZING HORMONE; PROGESTERONE;

EID: 77954973345     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2010.02.013     Document Type: Article
Times cited : (18)

References (13)
  • 1
    • 33646517073 scopus 로고    scopus 로고
    • X-linked premature failure: A complex disease
    • D. Toniolo X-linked premature failure: a complex disease Curr Opin Genet Dev 16 2006 293 300
    • (2006) Curr Opin Genet Dev , vol.16 , pp. 293-300
    • Toniolo, D.1
  • 2
    • 0025092789 scopus 로고
    • The critical region on the human Xq
    • E. Therman, R. Laxova, and B. Susman The critical region on the human Xq Genetics 85 1990 455 461
    • (1990) Genetics , vol.85 , pp. 455-461
    • Therman, E.1    Laxova, R.2    Susman, B.3
  • 3
    • 34147154179 scopus 로고    scopus 로고
    • Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: A hypothesis
    • F. Rizzolio, C. Sala, S. Alboresi, S. Bione, S. Gilli, and M. Goegan Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: a hypothesis Hum Genet 121 2007 441 450
    • (2007) Hum Genet , vol.121 , pp. 441-450
    • Rizzolio, F.1    Sala, C.2    Alboresi, S.3    Bione, S.4    Gilli, S.5    Goegan, M.6
  • 4
    • 0026678490 scopus 로고
    • Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
    • R.C. Allen, H.Y. Zoghbi, A.B. Moseley, H.M. Rosenblatt, and J.W. Belmont Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation Am J Hum Genet 51 1992 1229 1239
    • (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
    • Allen, R.C.1    Zoghbi, H.Y.2    Moseley, A.B.3    Rosenblatt, H.M.4    Belmont, J.W.5
  • 5
    • 17344369363 scopus 로고    scopus 로고
    • A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: Evidence for conserved function in oogenesis and implications for human sterility
    • S. Bione, C. Sala, C. Manzini, G. Arrigo, O. Zuffardi, and S. Banfi A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility Am J Hum Genet 62 1998 533 541
    • (1998) Am J Hum Genet , vol.62 , pp. 533-541
    • Bione, S.1    Sala, C.2    Manzini, C.3    Arrigo, G.4    Zuffardi, O.5    Banfi, S.6
  • 6
    • 0036052632 scopus 로고    scopus 로고
    • Most X;autosome translocations associated with premature ovarian failure do not interrupt X-linked genes
    • R.L. Prueitt, H. Chen, R.I. Barnes, and A.R. Zinn Most X;autosome translocations associated with premature ovarian failure do not interrupt X-linked genes Cytogenet Genome Res 97 2002 32 38
    • (2002) Cytogenet Genome Res , vol.97 , pp. 32-38
    • Prueitt, R.L.1    Chen, H.2    Barnes, R.I.3    Zinn, A.R.4
  • 7
    • 19944401523 scopus 로고    scopus 로고
    • Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B
    • S. Bione, F. Rizzolio, C. Sala, R. Ricotti, M. Goegan, and M.C. Mancini Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B Hum Reprod 19 2004 2759 2766
    • (2004) Hum Reprod , vol.19 , pp. 2759-2766
    • Bione, S.1    Rizzolio, F.2    Sala, C.3    Ricotti, R.4    Goegan, M.5    Mancini, M.C.6
  • 10
    • 0023908744 scopus 로고
    • The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes
    • R.M. Speed The possible role of meiotic pairing anomalies in the atresia of human fetal oocytes Hum Genet 78 1988 260 266
    • (1988) Hum Genet , vol.78 , pp. 260-266
    • Speed, R.M.1
  • 11
    • 33646496697 scopus 로고    scopus 로고
    • Chromosomal rearrangements in Xq and premature ovarian failure: Mapping of 25 new cases and review of the literature
    • F. Rizzolio, S. Bione, C. Sala, M. Goegan, M. Gentile, and G. Gregato Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature Hum Reprod 21 2006 1477 1483
    • (2006) Hum Reprod , vol.21 , pp. 1477-1483
    • Rizzolio, F.1    Bione, S.2    Sala, C.3    Goegan, M.4    Gentile, M.5    Gregato, G.6
  • 12
    • 0035908996 scopus 로고    scopus 로고
    • NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation
    • L. Jun, S. Frints, H. Duhamel, A. Herold, J. Abad-Rodrigues, and C. Dotti NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation Curr Biol 11 2001 1381 1391
    • (2001) Curr Biol , vol.11 , pp. 1381-1391
    • Jun, L.1    Frints, S.2    Duhamel, H.3    Herold, A.4    Abad-Rodrigues, J.5    Dotti, C.6
  • 13
    • 10744222468 scopus 로고    scopus 로고
    • Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: Clinical study and mutation analysis of the NXF5 gene
    • S.G.M. Frints, L. Jun, J.P. Fryns, K. Devriendt, R. Teulingkx, and L. Van den Berghe Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene Am J Med Genet 119A 2003 367 374
    • (2003) Am J Med Genet , vol.119 , pp. 367-374
    • Frints, S.G.M.1    Jun, L.2    Fryns, J.P.3    Devriendt, K.4    Teulingkx, R.5    Van Den Berghe, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.