405 related articles for article (PubMed ID: 22513983)
21. Is chromosome analysis mandatory in the initial investigation of normovulatory women seeking infertility treatment?
Papanikolaou EG; Vernaeve V; Kolibianakis E; Assche EV; Bonduelle M; Liebaers I; Van Steirteghem A; Devroey P
Hum Reprod; 2005 Oct; 20(10):2899-903. PubMed ID: 15958396
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF).
Qin Y; Zhao H; Xu J; Shi Y; Li Z; Qiao J; Liu J; Qin C; Ren C; Li J; Chen S; Cao Y; ; Simpson JL; Chen ZJ
Hum Mol Genet; 2012 Jan; 21(2):430-6. PubMed ID: 21989058
[TBL] [Abstract][Full Text] [Related]
24. Frequency and types of chromosomal abnormalities in Turkish women with amenorrhea.
Demirhan O; Tanrıverdi N; Tunç E; Inandıklıoğlu N; Süleymanova D
J Pediatr Adolesc Gynecol; 2014 Oct; 27(5):274-7. PubMed ID: 25023981
[TBL] [Abstract][Full Text] [Related]
25. Clinical analysis of Chinese infertility women with premature ovarian failure.
Zhang P; Shi Y; Gao X; Wang S; Wang J; Chen ZJ
Neuro Endocrinol Lett; 2007 Oct; 28(5):580-4. PubMed ID: 17984952
[TBL] [Abstract][Full Text] [Related]
26. [Genetic anomalies in dysmenorrhea and sterility: range and frequency, age-related dependence, mosaicism dynamics].
Sazonova LA; Suskov II
Genetika; 1983; 19(1):171-3. PubMed ID: 6682067
[TBL] [Abstract][Full Text] [Related]
27. X chromosome mosaicism in patients with recurrent abortion or premature ovarian failure.
Wu RC; Kuo PL; Lin SJ; Liu CH; Tzeng CC
J Formos Med Assoc; 1993 Nov; 92(11):953-6. PubMed ID: 7910065
[TBL] [Abstract][Full Text] [Related]
28. Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.
Kleczkowska A; Dmoch E; Kubien E; Fryns JP; Van den Berghe H
Genet Couns; 1990; 1(3-4):227-33. PubMed ID: 2098046
[TBL] [Abstract][Full Text] [Related]
29. Prevalence of chromosomal abnormalities in Sri Lankan women with primary amenorrhea.
Samarakoon L; Sirisena ND; Wettasinghe KT; Kariyawasam KW; Jayasekara RW; Dissanayake VH
J Obstet Gynaecol Res; 2013 May; 39(5):991-7. PubMed ID: 23279116
[TBL] [Abstract][Full Text] [Related]
30. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA; Priest JH
Prenat Diagn; 1996 Jan; 16(1):1-28. PubMed ID: 8821848
[TBL] [Abstract][Full Text] [Related]
31. Premature ovarian failure.
Beck-Peccoz P; Persani L
Orphanet J Rare Dis; 2006 Apr; 1():9. PubMed ID: 16722528
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Cytogenetic analysis of patients with primary amenorrhea in Eastern India.
Ghosh S; Roy S; Pal P; Dutta A; Halder A
J Obstet Gynaecol; 2018 Feb; 38(2):270-275. PubMed ID: 29022424
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Chromosomal abnormalities in amenorrhea: a retrospective study and review of 637 patients in South India.
Dutta UR; Ponnala R; Pidugu VK; Dalal AB
Arch Iran Med; 2013 May; 16(5):267-70. PubMed ID: 23641739
[TBL] [Abstract][Full Text] [Related]
36. Mosaic pentasomy X/tetrasomy X syndrome and premature ovarian failure.
Wood A; Kleis L; Toriello H; Cemeroglu AP
Indian Pediatr; 2011 May; 48(5):402-4. PubMed ID: 21654007
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. A clinical and cytogenetic study of Turner syndrome.
Suri M; Kabra M; Jain U; Sanders V; Saxena R; Shukla A; Singh GV; Verma IC
Indian Pediatr; 1995 Apr; 32(4):433-42. PubMed ID: 8635807
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. [The most frequent chromosomal abnormalities in karyotypes of patients with reproductive problems].
Tavokina LV; Baronova EV; Sopko NI
Tsitol Genet; 2007; 41(4):48-55. PubMed ID: 18030726
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
