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Journal Abstract Search
259 related items for PubMed ID: 10727994
21. The X chromosome and the ovary. Zinn AR. J Soc Gynecol Investig; 2001; 8(1 Suppl Proceedings):S34-6. PubMed ID: 11223369 [Abstract] [Full Text] [Related]
22. 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 [Abstract] [Full Text] [Related]
26. Molecular analysis of genes on Xp controlling Turner syndrome and premature ovarian failure (POF). Zinn AR, Ross JL. Semin Reprod Med; 2001 Jun; 19(2):141-6. PubMed ID: 11480911 [Abstract] [Full Text] [Related]
27. 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 [Abstract] [Full Text] [Related]
28. [Premature ovarian insufficiency]. Christin-Maitre S. Rev Prat; 1999 Jun 15; 49(12):1297-302. PubMed ID: 10488661 [Abstract] [Full Text] [Related]
29. Del (X)(p21.2) in a mother and two daughters with variable ovarian function. Zinn AR, Ouyang B, Ross JL, Varma S, Bourgeois M, Tonk V. Clin Genet; 1997 Oct 15; 52(4):235-9. PubMed ID: 9383030 [Abstract] [Full Text] [Related]
30. Genetics of premature ovarian failure. Meczekalski B, Podfigurna-Stopa A. Minerva Endocrinol; 2010 Dec 15; 35(4):195-209. PubMed ID: 21178916 [Abstract] [Full Text] [Related]
31. Candidate genes for premature ovarian failure. Suzumori N, Pangas SA, Rajkovic A. Curr Med Chem; 2007 Dec 15; 14(3):353-7. PubMed ID: 17305537 [Abstract] [Full Text] [Related]
34. Short stature and primary ovarian insufficiency possibly due to chromosomal position effect in a balanced X;1 translocation. Genesio R, Mormile A, Licenziati MR, De Brasi D, Leone G, Balzano S, Izzo A, Bonfiglio F, Conti A, Fioretti G, Lenta S, Poggiano MR, Siani P, Nitsch L. Mol Cytogenet; 2015 Dec 15; 8():50. PubMed ID: 26175800 [Abstract] [Full Text] [Related]
38. A familial case of X chromosome deletion ascertained by cytogenetic screening of women with premature ovarian failure. Davison RM, Quilter CR, Webb J, Murray A, Fisher AM, Valentine A, Serhal P, Conway GS. Hum Reprod; 1998 Nov 15; 13(11):3039-41. PubMed ID: 9853851 [Abstract] [Full Text] [Related]