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Items: 1 to 20 of 85

1.

Evidence for the existence of the human "super female".

JACOBS PA, BAIKIE AG, BROWN WM, MACGREGOR TN, MACLEAN N, HARNDEN DG.

Lancet. 1959 Sep 26;2(7100):423-5. No abstract available.

PMID:
14406377
2.

[ON TRISOMY OF THE X-CHROMOSOME. (SO-CALLED TRIPLE X-SYNDROME OR SUPER FEMALE SYNDROME)].

HIENZ HA, MICHAEL CM, SCHULZ FW, WALTER K.

Klin Wochenschr. 1963 Oct 15;41:996-1001. German. No abstract available.

PMID:
14094388
3.

The XXX syndrome frequency among mental defectives and fertility.

FRASER JH, CAMPBELL J, MACGILLIVRAY RC, BOYD E, LENNOX B.

Lancet. 1960 Sep 17;2(7151):626-7. No abstract available.

PMID:
13701513
4.

TWO APPARENTLY NORMAL TRIPLE-X FEMALES.

CLOSE HG.

Lancet. 1963 Dec 28;2(7322):1358-9. No abstract available.

PMID:
14071151
5.

The triple-X syndrome. Clinical, pathological, and chromosomal studies in three mentally retarded cases.

JOHNSTON AW, FERGUSON-SMITH MA, HANDMAKER SD, JONES HW, JONES GS.

Br Med J. 1961 Oct 21;2(5259):1046-52. No abstract available.

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
7.

[Double aneuploidy (trisomy X, trisomy 18) in a newborn with trisomy 18 phenotype].

Pachajoa H.

Arch Argent Pediatr. 2013 Jul-Aug;111(4):e101-4. doi: 10.1590/S0325-00752013000400019. Review. Spanish.

8.

Triple X syndrome.

Afshan A.

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

9.

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
10.

Genotyping by morphology...

Wondergem MJ, Ossenkoppele GJ.

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

11.

Maternal 47,XX,i(X)(q10) as a cause of false positive sex chromosome aneuploidy in noninvasive prenatal screening.

DeMaio A, Green A, Daly S.

Prenat Diagn. 2016 Jul;36(7):693-5. doi: 10.1002/pd.4838. Epub 2016 Jun 7. No abstract available.

PMID:
27152665
12.

[Gastrointestinal obstruction in the mosaic trisomy X].

Cammarata-Scalisi F, Araque D, Stock F, Molina M, Rodríguez R, Vázquez G, Cammarata-Scalisi G, Cammarata-Scalisi ME.

Acta Gastroenterol Latinoam. 2015 Jun;45(2):129-32. Spanish.

PMID:
26353463
13.

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.

14.

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
15.

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
16.

Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.

Porreco RP, Garite TJ, Maurel K, Marusiak B; Obstetrix Collaborative Research Network, Ehrich M, van den Boom D, Deciu C, Bombard A.

Am J Obstet Gynecol. 2014 Oct;211(4):365.e1-12. doi: 10.1016/j.ajog.2014.03.042. Epub 2014 Mar 19.

PMID:
24657131
17.

[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.

18.

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
19.

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
20.

Trisomy-X with estrous cycle anomalies in two female dogs.

O'Connor CL, Schweizer C, Gradil C, Schlafer D, Lopate C, Prociuk U, Meyers-Wallen VN, Casal ML.

Theriogenology. 2011 Jul 15;76(2):374-80. doi: 10.1016/j.theriogenology.2011.02.017. Epub 2011 May 7.

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