152 related articles for article (PubMed ID: 16239311)
1. 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. PubMed ID: 16239311
[TBL] [Abstract][Full Text] [Related]
2. A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28.
Rossetti F; Rizzolio F; Pramparo T; Sala C; Bione S; Bernardi F; Goegan M; Zuffardi O; Toniolo D
Eur J Hum Genet; 2004 Oct; 12(10):829-34. PubMed ID: 15280899
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 19524892
[TBL] [Abstract][Full Text] [Related]
4. Cryptic Xp duplication including the SHOX gene in a woman with 46,X, del(X)(q21.31) and premature ovarian failure.
Tachdjian G; Aboura A; Portnoï MF; Pasquier M; Bourcigaux N; Simon T; Rousseau G; Finkel L; Benkhalifa M; Christin-Maitre S
Hum Reprod; 2008 Jan; 23(1):222-6. PubMed ID: 17981816
[TBL] [Abstract][Full Text] [Related]
5. X-chromosome abnormalities in women with premature ovarian failure.
Devi A; Benn PA
J Reprod Med; 1999 Apr; 44(4):321-4. PubMed ID: 10319299
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 16751643
[TBL] [Abstract][Full Text] [Related]
7. Novel X-chromosomal defect associated with abnormal ovarian function.
Rao L; Babu A; Padmalatha V; Kanakavalli M; Deenadayal M; Singh L
J Obstet Gynaecol Res; 2005 Feb; 31(1):12-5. PubMed ID: 15669985
[TBL] [Abstract][Full Text] [Related]
8. Unbalanced translocation in an adult patient with premature ovarian failure and mental retardation detected by spectral karyotyping and array-comparative genomic hybridization.
Guo QS; Qin SY; Zhou SF; He L; Ma D; Zhang YP; Xiong Y; Peng T; Cheng Y; Li XT
Eur J Clin Invest; 2009 Aug; 39(8):729-37. PubMed ID: 19515099
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.
Kim MK; Seok HH; Kim YS; Chin MU; Sung SR; Lee WS; Shim SH; Yoon TK
Gene; 2014 Jan; 534(1):54-9. PubMed ID: 24148559
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 20170342
[TBL] [Abstract][Full Text] [Related]
11. 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; 52(1):19-26. PubMed ID: 7977456
[TBL] [Abstract][Full Text] [Related]
12. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
Lose F; Duffy DL; Kay GF; Kedda MA; Spurdle AB; ;
J Natl Cancer Inst; 2008 Nov; 100(21):1519-29. PubMed ID: 18957670
[TBL] [Abstract][Full Text] [Related]
13. Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.
Miano MG; Laperuta C; Chiurazzi P; D'Urso M; Ursini MV
BMC Med Genet; 2007 Apr; 8():18. PubMed ID: 17428316
[TBL] [Abstract][Full Text] [Related]
14. Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.
Bodega B; Bione S; Dalprà L; Toniolo D; Ornaghi F; Vegetti W; Ginelli E; Marozzi A
Hum Reprod; 2006 Apr; 21(4):952-7. PubMed ID: 16361284
[TBL] [Abstract][Full Text] [Related]
15. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome.
Wimplinger I; Rauch A; Orth U; Schwarzer U; Trautmann U; Kutsche K
Eur J Med Genet; 2007; 50(6):421-31. PubMed ID: 17845869
[TBL] [Abstract][Full Text] [Related]
16. Aetiology of premature ovarian failure.
Vujovic S
Menopause Int; 2009 Jun; 15(2):72-5. PubMed ID: 19465673
[TBL] [Abstract][Full Text] [Related]
17. Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome.
Krauss CM; Turksoy RN; Atkins L; McLaughlin C; Brown LG; Page DC
N Engl J Med; 1987 Jul; 317(3):125-31. PubMed ID: 3600701
[TBL] [Abstract][Full Text] [Related]
18. Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inactivation pattern.
Rodriguez-Revenga L; Madrigal I; Badenas C; Xunclà M; Jiménez L; Milà M
Menopause; 2009; 16(5):944-9. PubMed ID: 19373114
[TBL] [Abstract][Full Text] [Related]
19. 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 Aug; 94(3):1097.e5-8. PubMed ID: 20338563
[TBL] [Abstract][Full Text] [Related]
20. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
Marozzi A; Manfredini E; Tibiletti MG; Furlan D; Villa N; Vegetti W; Crosignani PG; Ginelli E; Meneveri R; Dalprà L
Hum Genet; 2000 Oct; 107(4):304-11. PubMed ID: 11129329
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
