351 related articles for article (PubMed ID: 19837940)
1. Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.
Aboura A; Dupas C; Tachdjian G; Portnoï MF; Bourcigaux N; Dewailly D; Frydman R; Fauser B; Ronci-Chaix N; Donadille B; Bouchard P; Christin-Maitre S
J Clin Endocrinol Metab; 2009 Nov; 94(11):4540-6. PubMed ID: 19837940
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. Analysis of Chinese women with primary ovarian insufficiency by high resolution array-comparative genomic hybridization.
Liao C; Fu F; Yang X; Sun YM; Li DZ
Chin Med J (Engl); 2011 Jun; 124(11):1739-42. PubMed ID: 21740789
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 20570974
[TBL] [Abstract][Full Text] [Related]
6. Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.
McGuire MM; Bowden W; Engel NJ; Ahn HW; Kovanci E; Rajkovic A
Fertil Steril; 2011 Apr; 95(5):1595-600. PubMed ID: 21256485
[TBL] [Abstract][Full Text] [Related]
7. Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases.
Tšuiko O; Nõukas M; Žilina O; Hensen K; Tapanainen JS; Mägi R; Kals M; Kivistik PA; Haller-Kikkatalo K; Salumets A; Kurg A
Hum Reprod; 2016 Aug; 31(8):1913-25. PubMed ID: 27301361
[TBL] [Abstract][Full Text] [Related]
8. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
[TBL] [Abstract][Full Text] [Related]
9. [Analysis of genomic copy number variations in two sisters with primary amenorrhea and hyperandrogenism].
Zhang Y; Xu Q; Cai X; Li Y; Song G; Wang J; Zhang R; Dai Y; Duan Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):814-8. PubMed ID: 26663055
[TBL] [Abstract][Full Text] [Related]
10. Genomic changes detected by array CGH in human embryos with developmental defects.
Rajcan-Separovic E; Qiao Y; Tyson C; Harvard C; Fawcett C; Kalousek D; Stephenson M; Philipp T
Mol Hum Reprod; 2010 Feb; 16(2):125-34. PubMed ID: 19778950
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
[TBL] [Abstract][Full Text] [Related]
18. Copy number variants in premature ovarian failure and ovarian dysgenesis.
Ledig S; Röpke A; Wieacker P
Sex Dev; 2010 Sep; 4(4-5):225-32. PubMed ID: 20606390
[TBL] [Abstract][Full Text] [Related]
19. [Usefulness of CGH-array and SNP-array for the etiological diagnosis of premature ovarian insufficiency].
Hyon C
Biol Aujourdhui; 2017; 211(3):199-205. PubMed ID: 29412129
[TBL] [Abstract][Full Text] [Related]
20. Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure.
Dudding TE; Lawrence O; Winship I; Froyen G; Vandewalle J; Scott R; Shelling AN
Hum Reprod; 2010 Dec; 25(12):3159-60; author reply 3160-1. PubMed ID: 20952765
[No Abstract] [Full Text] [Related]
[Next] [New Search]