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Similar articles for PubMed (Select 12199336)

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.

Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX.

Samango-Sprouse C, Keen C, Mitchell F, Sadeghin T, Gropman A.

Am J Med Genet A. 2015 Jun 18. doi: 10.1002/ajmg.a.37198. [Epub ahead of print]

PMID:
26086740
3.

Premature ovarian failure due to tetrasomy X in an adolescent girl.

Kara C, Üstyol A, Yılmaz A, Altundağ E, Oğur G.

Eur J Pediatr. 2014 Dec;173(12):1627-30. doi: 10.1007/s00431-013-2209-y. Epub 2013 Nov 13.

PMID:
24221609
4.

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.

PMID:
21654007
5.

[Phenotypic variability in 47, XXX patients: Clinical report of four new cases].

Goldschmidt E, Márquez M, Solari A, Ziembar MI, Laudicina A.

Arch Argent Pediatr. 2010 Aug;108(4):e88-91. doi: 10.1590/S0325-00752010000400012. Spanish.

6.

Chromosomal abnormalities in women with premature ovarian failure.

Artini PG, Ruggiero M, Papini F, Valentino V, Uccelli A, Cela V, Genazzani AR.

Gynecol Endocrinol. 2010 Oct;26(10):717-24. doi: 10.3109/09513590.2010.500427. Review.

PMID:
20653407
7.

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
8.

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.

9.

Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy.

Ottesen AM, Aksglaede L, Garn I, Tartaglia N, Tassone F, Gravholt CH, Bojesen A, Sørensen K, Jørgensen N, Rajpert-De Meyts E, Gerdes T, Lind AM, Kjaergaard S, Juul A.

Am J Med Genet A. 2010 May;152A(5):1206-12. doi: 10.1002/ajmg.a.33334.

PMID:
20425825
10.

The clinical effects of isochromosome Xq in Klinefelter syndrome: report of a case and review of literature.

Demirhan O, Pazarbaşi A, Tanriverdi N, Aridoğan A, Karahan D.

Genet Couns. 2009;20(3):235-42. Review.

PMID:
19852429
11.

Long-term growth hormone therapy in an adolescent boy with 45,X/46,XidicY(p11).

Guevarra FM, Nimkarn S, New MI, Lin-Su K.

J Pediatr. 2009 Nov;155(5):752-5.e1-3. doi: 10.1016/j.jpeds.2009.03.018.

PMID:
19840619
12.

X;7 translocation in an Indian woman with hypergonadotropic amenorrhea-a case report.

Vasu VR, Chandra N, Santhiya ST.

Genet Test Mol Biomarkers. 2009 Aug;13(4):533-6. doi: 10.1089/gtmb.2009.0051.

PMID:
19663602
13.

Turner syndrome and 45,X/47,XXX mosaicism.

Akbas E, Mutluhan H, Savasoglu K, Soylemez F, Ozturk I, Yazici G.

Genet Couns. 2009;20(2):141-6.

PMID:
19650411
14.

Triple X syndrome: a review of the literature.

Otter M, Schrander-Stumpel CT, Curfs LM.

Eur J Hum Genet. 2010 Mar;18(3):265-71. doi: 10.1038/ejhg.2009.109. Epub 2009 Jul 1. Review.

15.

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
16.

Aetiology of premature ovarian failure.

Vujovic S.

Menopause Int. 2009 Jun;15(2):72-5. doi: 10.1258/mi.2009.009020. Review.

PMID:
19465673
17.

Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failure.

Bachelot A, Rouxel A, Massin N, Dulon J, Courtillot C, Matuchansky C, Badachi Y, Fortin A, Paniel B, Lecuru F, Lefrère-Belda MA, Constancis E, Thibault E, Meduri G, Guiochon-Mantel A, Misrahi M, Kuttenn F, Touraine P; POF-GIS Study Group.

Eur J Endocrinol. 2009 Jul;161(1):179-87. doi: 10.1530/EJE-09-0231. Epub 2009 May 1.

18.

Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inactivation pattern.

Rodriguez-Revenga L, Madrigal I, Badenas C, Xunclà M, Jiménez L, Milà M.

Menopause. 2009 Sep-Oct;16(5):944-9. doi: 10.1097/gme.0b013e3181a06a37.

PMID:
19373114
19.

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
20.

Tall stature and poor breast development after estrogen replacement in a hypergonadotrophic hypogonadic patient with a 45,X/46,X,der(X) karyotype with SHOX gene overdosage.

Nishi MY, Correa RV, Costa EM, Billerbeck AE, Cruzes AL, Domenice S, Carvalho LR, Mendonca BB.

Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1282-7.

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