362 related articles for article (PubMed ID: 17482166)
1. 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. PubMed ID: 17482166
[TBL] [Abstract][Full Text] [Related]
2. Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.
Hernando C; Plaja A; Català V; Sarret E; Egozcue J; Fuster C
Fertil Steril; 2004 Dec; 82(6):1666-71. PubMed ID: 15589876
[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. 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]
5. Ectopic nucleolus organizer regions in a patient with premature ovarian failure.
Lloveras E; Zamora L; Pérez C; Fuster C; Andreu S; Plaja A
Fertil Steril; 2006 Oct; 86(4):1001.e15-6. PubMed ID: 17027366
[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. Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Chen CP; Lin CC; Li YC; Hsieh LJ; Lee CC; Wang W
Fertil Steril; 2006 Nov; 86(5):1514.e1-2. PubMed ID: 17070202
[TBL] [Abstract][Full Text] [Related]
8. Rapid generation of whole chromosome painting probes (WCPs) by chromosome microdissection.
Guan XY; Meltzer PS; Trent JM
Genomics; 1994 Jul; 22(1):101-7. PubMed ID: 7959755
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Molecular cytogenetic detection of minute chromosomal structural abnormality on the chromosomal terminal regions].
Tan YQ; Li LY; Lu GX
Yi Chuan Xue Bao; 2002 Sep; 29(9):753-6. PubMed ID: 12561219
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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. PubMed ID: 11035551
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Mosaic ring X chromosome in a case of secondary amenorrhea.
Chrisoulidou A; Bili H; Georgiou E; Mavroudi S; Lazaridou AS
Fertil Steril; 2008 Oct; 90(4):1198.e19-21. PubMed ID: 18177863
[TBL] [Abstract][Full Text] [Related]
15. Unusual pseudo dicentric, psu dic (1;19)(q10;q13.42), in a female with premature ovarian failure.
Northup J; Griffis K; Hawkins J; Lockhart L; Velagaleti G
Fertil Steril; 2007 Mar; 87(3):697.e5-8. PubMed ID: 17140574
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
Engelen JJ; Loots WJ; Albrechts JC; Plomp AS; van der Meer SB; Vles JS; Hamers GJ; Geraedts JP
Am J Med Genet; 1998 Feb; 75(4):409-13. PubMed ID: 9482648
[TBL] [Abstract][Full Text] [Related]
17. [Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization].
Zhu G; Bartsch O; Wan M; Gillessen-Kaesbach G; Passarge E
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):96-9. PubMed ID: 11295125
[TBL] [Abstract][Full Text] [Related]
18. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.
Valetto A; Bertini V; Rapalini E; Baldinotti F; Di Martino D; Simi P
Fertil Steril; 2004 May; 81(5):1388-90. PubMed ID: 15136108
[TBL] [Abstract][Full Text] [Related]
19. [Analysis of X chromosome mosaicism in patients with premature ovarian failure by fluorescent in-situ hybridization].
Diao FY; Xu M; Liu JY
Zhonghua Fu Chan Ke Za Zhi; 2003 Jan; 38(1):20-3. PubMed ID: 12757653
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
