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Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?
Lissoni S, Baronchelli S, Villa N, Lucchini V, Betri E, Cavalli P, Dalprà L.
Mol Cytogenet. 2009 Sep 27;2:19.PMID: 19781104 [PubMed - in process]Free PMC ArticleFree textRelated citations
Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure.
Cheng DH, Tan YQ, Di YF, Li LY, Lu GX.
Fertil Steril. 2009 Aug;92(2):828.e3-6. Epub 2009 Jun 13.PMID: 19524892 [PubMed - indexed for MEDLINE]Related citations
Skewed X-chromosome inactivation is associated with primary but not secondary ovarian failure.
Bretherick KL, Metzger DL, Chanoine JP, Panagiotopoulos C, Watson SK, Lam WL, Fluker MR, Brown CJ, Robinson WP.
Am J Med Genet A. 2007 May 1;143A(9):945-51.PMID: 17431892 [PubMed - indexed for MEDLINE]Related citations
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients.
Portnoï MF, Aboura A, Tachdjian G, Bouchard P, Dewailly D, Bourcigaux N, Frydman R, Reyss AC, Brisset S, Christin-Maitre S.
Hum Reprod. 2006 Sep;21(9):2329-34. Epub 2006 Jun 3.PMID: 16751643 [PubMed - indexed for MEDLINE]Free ArticleRelated citations
X-chromosome abnormalities in women with premature ovarian failure.
Devi A, Benn PA.
J Reprod Med. 1999 Apr;44(4):321-4.PMID: 10319299 [PubMed - indexed for MEDLINE]Related citations
Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients.
Lakhal B, Braham R, Berguigua R, Bouali N, Zaouali M, Chaieb M, Veitia RA, Saad A, Elghezal H.
Clin Genet. 2010 Aug;78(2):181-5. Epub 2009 Dec 2.PMID: 20345472 [PubMed - in process]Related citations
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.
Ferreira SI, Matoso E, Pinto M, Almeida J, Liehr T, Melo JB, Carreira IM.
Mol Cytogenet. 2010 Jul 20;3(1):14. [Epub ahead of print]PMID: 20646274 [PubMed - as supplied by publisher]Free ArticleRelated citations
Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection.
Weimer J, Shivakumar S, Danda S, Thomas N, Ralui LP, Jonat W, Arnold N.
Fertil Steril. 2007 Dec;88(6):1677.e9-13. Epub 2007 May 7.PMID: 17482166 [PubMed - indexed for MEDLINE]Related citations
Epigenetic analysis of the critical region I for premature ovarian failure: demonstration of a highly heterochromatic domain on the long arm of the mammalian X chromosome.
Rizzolio F, Pramparo T, Sala C, Zuffardi O, De Santis L, Rabellotti E, Calzi F, Fusi F, Bellazzi R, Toniolo D.
J Med Genet. 2009 Sep;46(9):585-92. Epub 2008 Jul 15.PMID: 18628312 [PubMed - indexed for MEDLINE]Related citations
Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature.
Powell CM, Taggart RT, Drumheller TC, Wangsa D, Qian C, Nelson LM, White BJ.
Am J Med Genet. 1994 Aug 1;52(1):19-26. Review.PMID: 7977456 [PubMed - indexed for MEDLINE]Related citations
Molecular cytogenetic definition of a translocation t(X;15) associated with premature ovarian failure.
Bertini V, Ghirri P, Bicocchi MP, Simi P, Valetto A.
Fertil Steril. 2010 Mar 23. [Epub ahead of print]PMID: 20338563 [PubMed - as supplied by publisher]Related citations
X chromosome inactivation patterns in patients with idiopathic premature ovarian failure.
Yoon SH, Choi YM, Hong MA, Kang BM, Kim JJ, Min EG, Kim JG, Moon SY.
Hum Reprod. 2008 Mar;23(3):688-92. Epub 2008 Jan 8.PMID: 18182395 [PubMed - indexed for MEDLINE]Free ArticleRelated citations
Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X:Y translocation in a patient with secondary amenorrhoea.
Delon B, Lallaoui H, Abel-Lablanche C, Geneix A, Bellec V, Benkhalifa M.
Mol Hum Reprod. 1997 May;3(5):439-43.PMID: 9239729 [PubMed - indexed for MEDLINE]Free ArticleRelated citations
Skewed X chromosome inactivation may be not associated with premature ovarian failure.
Pu D, Wu J, Liu J.
Gynecol Endocrinol. 2010 Jun;26(6):423-8.PMID: 20170342 [PubMed - in process]Related citations
Most X;autosome translocations associated with premature ovarian failure do not interrupt X-linked genes.
Prueitt RL, Chen H, Barnes RI, Zinn AR.
Cytogenet Genome Res. 2002;97(1-2):32-8.PMID: 12438735 [PubMed - indexed for MEDLINE]Related citations
Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).
Quilter CR, Karcanias AC, Bagga MR, Duncan S, Murray A, Conway GS, Sargent CA, Affara NA.
Hum Reprod. 2010 Aug;25(8):2139-50. Epub 2010 Jun 22.PMID: 20570974 [PubMed - in process]Related citations
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature.
Rizzolio F, Bione S, Sala C, Goegan M, Gentile M, Gregato G, Rossi E, Pramparo T, Zuffardi O, Toniolo D.
Hum Reprod. 2006 Jun;21(6):1477-83. Epub 2006 Feb 23.PMID: 16497693 [PubMed - indexed for MEDLINE]Free ArticleRelated citations
Genetic significance of skewed X-chromosome inactivation in premature ovarian failure.
Sato K, Uehara S, Hashiyada M, Nabeshima H, Sugawara J, Terada Y, Yaegashi N, Okamura K.
Am J Med Genet A. 2004 Oct 15;130A(3):240-4.PMID: 15378546 [PubMed - indexed for MEDLINE]Related citations
Choroideremia, sensorineural deafness, and primary ovarian failure in a woman with a balanced X-4 translocation.
Lorda-Sanchez IJ, Ibañez AJ, Sanz RJ, Trujillo MJ, Anabitarte ME, Querejeta ME, Rodriguez de Alba M, Gimenez A, Infantes F, Ramos C, Garcia-Sandoval B, Ayuso C.
Ophthalmic Genet. 2000 Sep;21(3):185-9.PMID: 11035551 [PubMed - indexed for MEDLINE]Related citations
Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction.
Fimiani G, Laperuta C, Falco G, Ventruto V, D'Urso M, Ursini MV, Miano MG.
Hum Reprod. 2006 Feb;21(2):529-35. Epub 2005 Oct 20.PMID: 16239311 [PubMed - indexed for MEDLINE]Free ArticleRelated citations
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