173 related articles for article (PubMed ID: 21150920)
1. Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure.
Nishimura-Tadaki A; Wada T; Bano G; Gough K; Warner J; Kosho T; Ando N; Hamanoue H; Sakakibara H; Nishimura G; Tsurusaki Y; Doi H; Miyake N; Wakui K; Saitsu H; Fukushima Y; Hirahara F; Matsumoto N
J Hum Genet; 2011 Feb; 56(2):156-60. PubMed ID: 21150920
[TBL] [Abstract][Full Text] [Related]
2. Cytogenetic analysis of 531 Chinese women with premature ovarian failure.
Jiao X; Qin C; Li J; Qin Y; Gao X; Zhang B; Zhen X; Feng Y; Simpson JL; Chen ZJ
Hum Reprod; 2012 Jul; 27(7):2201-7. PubMed ID: 22513983
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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. PubMed ID: 12438735
[TBL] [Abstract][Full Text] [Related]
5. Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene.
Prueitt RL; Ross JL; Zinn AR
Cytogenet Cell Genet; 2000; 89(1-2):44-50. PubMed ID: 10894934
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of de novo X;autosome translocations.
Abrams L; Cotter PD
Clin Genet; 2004 May; 65(5):423-8. PubMed ID: 15099352
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Translocation t(X;11)(q22;q25) in a woman with premature ovarian failure.
Saranya B; Kavitha Devi D; Chandra RS; Jayashankar M; Santhiya ST
Sex Dev; 2013; 7(4):216-21. PubMed ID: 23429171
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.
Ochalski ME; Engle N; Wakim A; Ravnan BJ; Hoffner L; Rajkovic A; Surti U
Fertil Steril; 2011 Jun; 95(7):2433.e9-15. PubMed ID: 21530964
[TBL] [Abstract][Full Text] [Related]
11. Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations.
Moysés-Oliveira M; Guilherme Rdos S; Dantas AG; Ueta R; Perez AB; Haidar M; Canonaco R; Meloni VA; Kosyakova N; Liehr T; Carvalheira GM; Melaragno MI
Fertil Steril; 2015 May; 103(5):1289-96.e2. PubMed ID: 25747126
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic analysis of 179 Iranian women with premature ovarian failure.
Kalantari H; Madani T; Zari Moradi S; Mansouri Z; Almadani N; Gourabi H; Mohseni Meybodi A
Gynecol Endocrinol; 2013 Jun; 29(6):588-91. PubMed ID: 23656387
[TBL] [Abstract][Full Text] [Related]
14. Epigenetic control of the critical region for premature ovarian failure on autosomal genes translocated to the X chromosome: a hypothesis.
Rizzolio F; Sala C; Alboresi S; Bione S; Gilli S; Goegan M; Pramparo T; Zuffardi O; Toniolo D
Hum Genet; 2007 May; 121(3-4):441-50. PubMed ID: 17265046
[TBL] [Abstract][Full Text] [Related]
15. Chromatin structural elements and chromosomal translocations in leukemia.
Zhang Y; Rowley JD
DNA Repair (Amst); 2006 Sep; 5(9-10):1282-97. PubMed ID: 16893685
[TBL] [Abstract][Full Text] [Related]
16. Premature ovarian failure.
Beck-Peccoz P; Persani L
Orphanet J Rare Dis; 2006 Apr; 1():9. PubMed ID: 16722528
[TBL] [Abstract][Full Text] [Related]
17. A teenager with a t(X;17)(q22;q25) and ovarian failure.
Martínez-Valenzuela M; Rivera H; Mundo-Ayala JN; González-Mercado MG; Davalos-Rodríguez IP
Genet Couns; 2010; 21(3):269-75. PubMed ID: 20964116
[TBL] [Abstract][Full Text] [Related]
18. Genetic aspects of premature ovarian failure: a literature review.
Cordts EB; Christofolini DM; Dos Santos AA; Bianco B; Barbosa CP
Arch Gynecol Obstet; 2011 Mar; 283(3):635-43. PubMed ID: 21188402
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 16497693
[TBL] [Abstract][Full Text] [Related]
20. Genetics of premature ovarian failure.
Meczekalski B; Podfigurna-Stopa A
Minerva Endocrinol; 2010 Dec; 35(4):195-209. PubMed ID: 21178916
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]