PubMed

A Turner syndrome neurocognitive phenotype maps to Xp22.3.

Zinn AR, Roeltgen D, Stefanatos G, Ramos P, Elder FF, Kushner H, Kowal K, Ross JL.

Behav Brain Funct. 2007 May 21;3:24.PMID: 17517138 [PubMed]Related articlesFree article

The Turner syndrome-associated neurocognitive phenotype maps to distal Xp.

Ross JL, Roeltgen D, Kushner H, Wei F, Zinn AR.

Am J Hum Genet. 2000 Sep;67(3):672-81. Epub 2000 Aug 8.PMID: 10931762 [PubMed - indexed for MEDLINE]Related articlesFree article

Cognition and the sex chromosomes: studies in Turner syndrome.

Ross J, Roeltgen D, Zinn A.

Horm Res. 2006;65(1):47-56. Epub 2006 Jan 4. Review.PMID: 16397401 [PubMed - indexed for MEDLINE]Related articles

Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.

Ogata T, Muroya K, Matsuo N, Shinohara O, Yorifuji T, Nishi Y, Hasegawa Y, Horikawa R, Tachibana K.

J Clin Endocrinol Metab. 2001 Nov;86(11):5498-508.PMID: 11701728 [PubMed - indexed for MEDLINE]Related articlesFree article

Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location.

Boucher CA, Sargent CA, Ogata T, Affara NA.

J Med Genet. 2001 Sep;38(9):591-8.PMID: 11546827 [PubMed - indexed for MEDLINE]Related articlesFree article

Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26).

Reinehr T, Jauch A, Zoll B, Engel U, Bartels I, Andler W.

Am J Med Genet. 2001 Jul 22;102(1):81-5.PMID: 11471178 [PubMed - indexed for MEDLINE]Related articles

Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency.

Rappold G, Blum WF, Shavrikova EP, Crowe BJ, Roeth R, Quigley CA, Ross JL, Niesler B.

J Med Genet. 2007 May;44(5):306-13. Epub 2006 Dec 20.PMID: 17182655 [PubMed - indexed for MEDLINE]Related articlesFree article

SHOX intragenic microsatellite analysis in patients with short stature.

Ezquieta B, Cueva E, Oliver A, Gracia R.

J Pediatr Endocrinol Metab. 2002 Feb;15(2):139-48.PMID: 11874178 [PubMed - indexed for MEDLINE]Related articles

A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family.

Karaman B, Wollnik B, Ermiş H, Yüksel-Apak M, Başaran S.

Prenat Diagn. 2003 Apr;23(4):336-9.PMID: 12673642 [PubMed - indexed for MEDLINE]Related articles

The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.

Therman E, Susman B.

Hum Genet. 1990 Jul;85(2):175-83.PMID: 2370045 [PubMed - indexed for MEDLINE]Related articles

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

Zinn AR, Tonk VS, Chen Z, Flejter WL, Gardner HA, Guerra R, Kushner H, Schwartz S, Sybert VP, Van Dyke DL, Ross JL.

Am J Hum Genet. 1998 Dec;63(6):1757-66.PMID: 9837829 [PubMed - indexed for MEDLINE]Related articlesFree article

Trisomy of the short stature homeobox-containing gene (SHOX), resulting from a duplication-deletion of the X chromosome.

Adamson KA, Cross I, Batch JA, Rappold GA, Glass IA, Ball SG.

Clin Endocrinol (Oxf). 2002 May;56(5):671-5.PMID: 12035792 [PubMed - indexed for MEDLINE]Related articles

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.

Ergür AT, Ocal G, Berberoglu M, Tekin M, Kiliç BG, Aycan Z, Kutlu A, Adiyaman P, Siklar Z, Akar N, Sahin A, Akçayöz D.

Pediatr Int. 2008 Apr;50(2):172-4.PMID: 18353053 [PubMed - indexed for MEDLINE]Related articles

Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis.

Palka G, Stuppia L, Guanciali Franchi P, Chiarelli F, Fischetto R, Borrelli P, Giannotti A, Fioretti G, Rinaldi MM, Mingarelli R, Rappold GA, Calabrese G.

Clin Genet. 2000 Jun;57(6):449-53.PMID: 10905666 [PubMed - indexed for MEDLINE]Related articles

Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.

Chocholska S, Rossier E, Barbi G, Kehrer-Sawatzki H.

Am J Med Genet A. 2006 Mar 15;140(6):604-10.PMID: 16470742 [PubMed - indexed for MEDLINE]Related articles

Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features.

Adachi M, Tachibana K, Asakura Y, Muroya K, Ogata T.

Hum Genet. 2000 Mar;106(3):306-10.PMID: 10798359 [PubMed - indexed for MEDLINE]Related articles

Molecular and cytogenetic analysis of familial Xp deletions.

Wandstrat AE, Conroy JM, Zurcher VL, Pasztor LM, Clark BA, Zackowski JL, Schwartz S.

Am J Med Genet. 2000 Sep 11;94(2):163-9.PMID: 10982973 [PubMed - indexed for MEDLINE]Related articles

The effect of genetic differences and ovarian failure: intact cognitive function in adult women with premature ovarian failure versus turner syndrome.

Ross JL, Stefanatos GA, Kushner H, Bondy C, Nelson L, Zinn A, Roeltgen D.

J Clin Endocrinol Metab. 2004 Apr;89(4):1817-22.PMID: 15070950 [PubMed - indexed for MEDLINE]Related articlesFree article

Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation.

Joseph M, Cantú ES, Pai GS, Willi SM, Papenhausen PR, Weiss L.

J Med Genet. 1996 Nov;33(11):906-11.PMID: 8950669 [PubMed - indexed for MEDLINE]Related articlesFree article

Neurodevelopmental and psychosocial aspects of Turner syndrome.

Ross J, Zinn A, McCauley E.

Ment Retard Dev Disabil Res Rev. 2000;6(2):135-41. Review.PMID: 10899807 [PubMed - indexed for MEDLINE]Related articles