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Results: 1 to 20 of 104

1.

Triple X syndrome.

Afshan A.

J Pak Med Assoc. 2012 Apr;62(4):392-4.

PMID:
22755288
[PubMed - indexed for MEDLINE]
2.

Undetected sex chromosome aneuploidy by chromosomal microarray.

Markus-Bustani K, Yaron Y, Goldstein M, Orr-Urtreger A, Ben-Shachar S.

Prenat Diagn. 2012 Nov;32(11):1117-8. doi: 10.1002/pd.3979. Epub 2012 Oct 4.

PMID:
23034780
[PubMed - indexed for MEDLINE]
3.

Fetal axillary cystic hygroma: a novel association with triple X syndrome.

Iskender C, Tarım E, Cok T, Yalcinkaya C, Kalaycı H, Sahin F.

Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):955-7. doi: 10.1002/bdra.23083. Epub 2012 Oct 26.

PMID:
23109196
[PubMed - indexed for MEDLINE]
4.

Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature.

Butnariu L, Rusu C, Caba L, Pânzaru M, Braha E, Grămescu M, Popescu R, Bujoranu C, Gorduza EV.

Rev Med Chir Soc Med Nat Iasi. 2013 Jul-Sep;117(3):714-21. Review.

PMID:
24502039
[PubMed - indexed for MEDLINE]
5.

Autism in association with Triple X syndrome.

Ali SI, Byrne N, Mulligan A.

Eur Child Adolesc Psychiatry. 2012 Apr;21(4):233-5. doi: 10.1007/s00787-012-0248-y. Epub 2012 Feb 4. No abstract available.

PMID:
22311144
[PubMed - indexed for MEDLINE]
6.

Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.

Yao H, Zhang L, Zhang H, Jiang F, Hu H, Chen F, Jiang H, Mu F, Zhao L, Liang Z, Wang W.

Prenat Diagn. 2012 Nov;32(11):1114-6. doi: 10.1002/pd.3946. Epub 2012 Aug 18. No abstract available.

PMID:
22903289
[PubMed - indexed for MEDLINE]
7.

A mother with variant Turner syndrome and two daughters with trisomy X: a case report.

Ramachandram S, Keng WT, Ariffin R, Ganesan V.

J Genet. 2013;92(2):313-6. No abstract available.

PMID:
23970090
[PubMed - indexed for MEDLINE]
Free Article
8.

[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.

PMID:
20672182
[PubMed - indexed for MEDLINE]
Free Article
9.

Triploidy without molar change presenting as severe pre-eclampsia and left ventricular failure at 15 weeks.

Anev I, Rajasri AG, Reddy K, Pillai M.

J Obstet Gynaecol. 2011 Oct;31(7):659-60. doi: 10.3109/01443615.2011.598966. No abstract available.

PMID:
21973144
[PubMed - indexed for MEDLINE]
10.

The psychiatric phenotype in triple X syndrome: new hypotheses illustrated in two cases.

Otter M, Schrander-Stumpel CT, Didden R, Curfs LM.

Dev Neurorehabil. 2012;15(3):233-8. doi: 10.3109/17518423.2012.655799.

PMID:
22582855
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Genotyping by morphology...

Wondergem MJ, Ossenkoppele GJ.

Blood. 2011 Mar 3;117(9):2566. No abstract available.

PMID:
21488251
[PubMed - indexed for MEDLINE]
Free Article
12.

Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report.

Kurtoğlu S, Atabek ME, Akçakuş M, Ozkul Y, Saatçi C.

Turk J Pediatr. 2004 Oct-Dec;46(4):377-9.

PMID:
15641277
[PubMed - indexed for MEDLINE]
Free Article
13.

Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX.

Ben Hamouda H, Mkacher N, Elghezal H, Bannour H, Kamoun M, Soua H, Saad A, Souissi MM, Sfar MT.

J Gynecol Obstet Biol Reprod (Paris). 2009 Nov;38(7):599-603. doi: 10.1016/j.jgyn.2009.08.003. Epub 2009 Sep 16.

PMID:
19762167
[PubMed - indexed for MEDLINE]
Free Article
14.

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. doi: 10.1007/s00404-010-1815-4. Epub 2010 Dec 29. Review.

PMID:
21188402
[PubMed - indexed for MEDLINE]
15.

BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1).

Schlade-Bartusiak K, Brown L, Lomax B, Bruyère H, Gillan T, Hamilton S, McGillivray B, Eydoux P.

Am J Med Genet A. 2012 Sep;158A(9):2322-7. doi: 10.1002/ajmg.a.35516. Epub 2012 Aug 6.

PMID:
22887799
[PubMed - indexed for MEDLINE]
16.

Marfan syndrome in a Triple-X girl: a new association?

Tinsa F, Karboul L, Chekib J, Hamouda S, Ben Jemaa L, Boussetta K, Bousnina S.

Tunis Med. 2010 Mar;88(3):203-6.

PMID:
20415197
[PubMed - indexed for MEDLINE]
Free Article
17.

In vitro fertilization surrogacy in rare coexisting Mayer-Rokitansky-Kuster-Hauser syndrome and triple X karyotype.

Raziel A, Friedler S, Gidoni Y, Ben-ami I, Strassburger D, Ron-El R.

Fertil Steril. 2011 Apr;95(5):1788.e11-3. doi: 10.1016/j.fertnstert.2010.11.020. Epub 2010 Dec 8.

PMID:
21144508
[PubMed - indexed for MEDLINE]
18.

Methylation profile of genes on the human X chromosome.

Kelkar A, Deobagkar D.

Epigenetics. 2010 Oct 1;5(7):612-8. doi: 10.4161/epi.5.7.12797. Epub 2010 Oct 1.

PMID:
20657171
[PubMed - indexed for MEDLINE]
Free Article
19.

Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosis.

Sifakis S, Anagnostopoulou K, Plastira K, Vrachnis N, Konstantinidou A, Sklavounou E.

Birth Defects Res A Clin Mol Teratol. 2012 Apr;94(4):245-8. doi: 10.1002/bdra.22867. Epub 2012 Jan 27.

PMID:
22282126
[PubMed - indexed for MEDLINE]
20.

X chromosomal abnormalities in Indian adolescent girls.

Ganguly BB, Sahni S.

Teratog Carcinog Mutagen. 2003;Suppl 1:245-53.

PMID:
12616615
[PubMed - indexed for MEDLINE]

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