187 related articles for article (PubMed ID: 23429171)
1. 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]
2. 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]
3. 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]
4. 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]
5. A case of 46,X,der(X)t(X;X)(q22.1;p11) Xq22.1-->Xqter in a 12-year-old girl with premature ovarian failure.
Merhi ZO; Roberts JL; Awonuga AO
Gynecol Obstet Invest; 2007; 63(3):137-9. PubMed ID: 17057399
[TBL] [Abstract][Full Text] [Related]
6. [Xq;Yq translocation in a patient with premature ovarian insufficiency].
Yang S; Zhang Y; Hu J; Hu R; Jia Z; Xi H; Wang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):942-945. PubMed ID: 32820504
[TBL] [Abstract][Full Text] [Related]
7. Microarray detection of a de novo der(X)t(X;11)(q28;p13) in a girl with premature ovarian failure and features of Beckwith-Wiedemann syndrome.
Han JY; Shin JH; Han MS; Je GH; Shaffer LG
J Hum Genet; 2006; 51(7):641-3. PubMed ID: 16708166
[TBL] [Abstract][Full Text] [Related]
8. Disruption of HDX gene in premature ovarian failure.
Okten G; Gunes S; Onat OE; Tukun A; Ozcelik T; Kocak I
Syst Biol Reprod Med; 2013 Aug; 59(4):218-22. PubMed ID: 23441923
[TBL] [Abstract][Full Text] [Related]
9. Low-level X chromosome mosaicism in women with sporadic premature ovarian failure.
Gersak K; Veble A
Reprod Biomed Online; 2011 Apr; 22(4):399-403. PubMed ID: 21334258
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3).
Ledig S; Preisler-Adams S; Morlot S; Liehr T; Wieacker P
Sex Dev; 2015; 9(2):86-90. PubMed ID: 25676666
[TBL] [Abstract][Full Text] [Related]
14. Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region.
Fusco F; Paciolla M; Chen E; Li X; Genesio R; Conti A; Jones J; Poeta L; Lioi MB; Ursini MV; Miano MG
Hum Reprod; 2011 Nov; 26(11):3186-96. PubMed ID: 21859812
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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. PubMed ID: 20345472
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Premature ovarian failure, absence of pubic and axillary hair with de novo 46,X,t(X;15)(q24;q26.3).
Giacomozzi C; Gullotta F; Federico G; Colapietro I; Nardone AM; Cianfarani S
Am J Med Genet A; 2010 May; 152A(5):1305-9. PubMed ID: 20425841
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
