Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 128

1.

Growth and ovarian function in girls with 48,XXXX karyotype--patient report and review of the literature.

Rooman RP, Van Driessche K, Du Caju MV.

J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):1051-5. Review.

PMID:
12199336
2.

Primary ovarian failure and deletions of the long arm of chromosome 3.

Nguyen T, McDonnell CM, Zacharin MR.

J Pediatr Endocrinol Metab. 2005 Oct;18(10):1013-7. Review.

PMID:
16355815
3.

Dicentric isochromosome X with premature ovarian failure: report of two cases.

Wu MH, Tzeng CC, Kuo PL.

J Formos Med Assoc. 1993 Sep;92(9):848-50.

PMID:
7904872
4.

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;13(11):3039-41.

5.

Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disorders.

Goswami R, Goswami D, Kabra M, Gupta N, Dubey S, Dadhwal V.

Fertil Steril. 2003 Oct;80(4):1052-4.

PMID:
14556833
6.

A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotype.

Skałba P, Cygal A, Gierzyńska Z.

Endokrynol Pol. 2010 Mar-Apr;61(2):217-9.

7.

X-chromosome abnormalities in women with premature ovarian failure.

Devi A, Benn PA.

J Reprod Med. 1999 Apr;44(4):321-4.

PMID:
10319299
8.

Genetic significance of skewed X-chromosome inactivation in premature ovarian failure.

Sato K, Uehara S, Hashiyada M, Nabeshima H, Sugawara J, Terada Y, Yaegashi N, Okamura K.

Am J Med Genet A. 2004 Oct 15;130A(3):240-4.

PMID:
15378546
9.

[The cytogenetics of premature ovarian failure].

Castillo S, López F, Tobella L, Salazar S, Daher V.

Rev Chil Obstet Ginecol. 1992;57(5):341-5. Spanish.

PMID:
1342464
10.

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. Epub 2006 May 18.

PMID:
16708166
11.

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.

PMID:
15669985
12.
13.

Evaluation of serum androgen levels in women with premature ovarian failure.

Benetti-Pinto CL, Bedone AJ, Magna LA.

Fertil Steril. 2005 Feb;83(2):508-10.

PMID:
15705407
14.

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.

PMID:
17070202
15.

Tall stature as presenting symptom in a girl with triple X syndrome.

Liebezeit BU, Rohrer TR, Singer H, Doerr HG.

J Pediatr Endocrinol Metab. 2003 Feb;16(2):233-5.

PMID:
12713263
16.

Genetic abnormalities in Turkish women with premature ovarian failure.

Ceylaner G, Altinkaya SO, Mollamahmutoglu L, Ceylaner S.

Int J Gynaecol Obstet. 2010 Aug;110(2):122-4. doi: 10.1016/j.ijgo.2010.03.023. Epub 2010 May 15.

PMID:
20471647
18.

Primary Ovarian Insufficiency: X chromosome defects and autoimmunity.

Persani L, Rossetti R, Cacciatore C, Bonomi M.

J Autoimmun. 2009 Aug;33(1):35-41. doi: 10.1016/j.jaut.2009.03.004. Epub 2009 Apr 5. Review.

PMID:
19346101
19.

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. Review.

PMID:
11480911
20.

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. doi: 10.1016/j.fertnstert.2008.07.014. Epub 2009 Jun 13.

PMID:
19524892
Items per page

Supplemental Content

Write to the Help Desk