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Items: 1 to 20 of 60

1.

Mortality and incidence in women with 47,XXX and variants.

Stochholm K, Juul S, Gravholt CH.

Am J Med Genet A. 2010 Feb;152A(2):367-72. doi: 10.1002/ajmg.a.33214.

PMID:
20101696
2.

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.

3.

Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases.

Brun JL, Gangbo F, Wen ZQ, Galant K, Taine L, Maugey-Laulom B, Roux D, Mangione R, Horovitz J, Saura R.

Prenat Diagn. 2004 Mar;24(3):213-8.

PMID:
15057956
4.

Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX.

Reish O, Berryman T, Cunningham TR, Sher C, Oetting WS.

Chromosome Res. 2004;12(2):125-32.

PMID:
15053482
5.

Turner syndrome phenotype with 47,XXX karyotype: further investigation warranted?

Wallerstein R, Musen E, McCarrier J, Aisenberg J, Chartoff A, Hutcheon RG, Tepperberg J, Pappenhausen P, Griffin S.

Am J Med Genet A. 2004 Feb 15;125A(1):106-7. No abstract available.

PMID:
14755478
6.

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
7.

Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation.

Hammer S, Dorrani N, Hartiala J, Stein S, Schanen NC.

Am J Med Genet A. 2003 Oct 15;122A(3):223-6.

PMID:
12966522
8.

Prenatal diagnosis of triple X using fetal cells obtained by endocervical lavage.

Xi Zhao X, Suzumori K, Sato T.

Prenat Diagn. 2003 Jul;23(7):549-51.

PMID:
12868080
9.

Trisomy 8 mosaicism in a patient born to a mother with 47,XXX.

Nucaro AL, Cao A, Faedda A, Crisponi G.

Am J Med Genet A. 2003 May 15;119A(1):85-6. No abstract available.

PMID:
12707966
10.

Congenital chylothorax associated with trisomy X.

Cardoso D, Tuna M, Abrantes M, dos Santos HG, Da Silva LJ.

Eur J Pediatr. 2001 Dec;160(12):743. No abstract available.

PMID:
11795685
11.

Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for high rates of pregnancy termination.

Sagi M, Meiner V, Reshef N, Dagan J, Zlotogora J.

Prenat Diagn. 2001 Jun;21(6):461-5.

PMID:
11438950
12.

Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors.

Thomas NS, Ennis S, Sharp AJ, Durkie M, Hassold TJ, Collins AR, Jacobs PA.

Hum Mol Genet. 2001 Feb 1;10(3):243-50.

PMID:
11159943
14.
15.

Histone H4 acetylation analyses in patients with polysomy X: implications for the mechanism of X inactivation.

Leal CA, Ayala-Madrigal ML, Figuera LE, Medina C.

Hum Genet. 1998 Jul;103(1):29-33.

PMID:
9737772
16.
17.

Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?

Butler MG, Hedges LK, Rogan PK, Seip JR, Cassidy SB, Moeschler JB.

Am J Med Genet. 1997 Oct 3;72(1):111-4. No abstract available.

PMID:
9295086
18.

Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients.

Lin HJ, Ndiforchu F, Patell S.

Am J Med Genet. 1993 Mar 15;45(6):761-3. Review.

PMID:
8456857
19.

11q- and constitutional X trisomy in a patient with M5b acute non-lymphocytic leukemia.

Bigazzi C, Galieni P, Scarinci R, Vivarelli R, Bucalossi A, Biancolini G, Falbo R, Vessichelli F, Dispensa E.

Haematologica. 1993 May-Jun;78(3):185-6.

PMID:
8375750
20.

The growth of XXX females: population-based studies.

Ratcliffe SG, Pan H, McKie M.

Ann Hum Biol. 1994 Jan-Feb;21(1):57-66.

PMID:
8147577

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