PubMed (cited) for id: 309510

Year	Number of Results
1988	1
1996	1
2002	4
2004	2
2006	1
2008	1
2024	0

1

Wallerstein R, Sugalski R, Cohn L, Jawetz R, Friez M. Wallerstein R, et al. Clin Neurol Neurosurg. 2008 Jun;110(6):631-4. doi: 10.1016/j.clineuro.2008.03.007. Epub 2008 May 6. Clin Neurol Neurosurg. 2008. PMID: 18462864

2

Genotype-phenotype associations for ARX gene duplication in X-linked mental retardation.

Szczaluba K, Nawara M, Poirier K, Pilch J, Gajdulewicz M, Spodar K, Chelly J, Bal J, Mazurczak T. Szczaluba K, et al. Neurology. 2006 Dec 12;67(11):2073-5. doi: 10.1212/01.wnl.0000247833.29314.5b. Epub 2006 Nov 2. Neurology. 2006. PMID: 17082467

3

Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARX.

Partington MW, Turner G, Boyle J, Gécz J. Partington MW, et al. Clin Genet. 2004 Jul;66(1):39-45. doi: 10.1111/j.0009-9163.2004.00268.x. Clin Genet. 2004. PMID: 15200506

4

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.

Kato M, Das S, Petras K, Kitamura K, Morohashi KI, Abuelo DN, Barr M, Bonneau D, Brady AF, Carpenter NJ, Cipero KL, Frisone F, Fukuda T, Guerrini R, Iida E, Itoh M, Lewanda AF, Nanba Y, Oka A, Proud VK, Saugier-Veber P, Schelley SL, Selicorni A, Shaner R, Silengo M, Stewart F, Sugiyama N, Toyama J, Toutain A, Vargas AL, Yanazawa M, Zackai EH, Dobyns WB. Kato M, et al. Hum Mutat. 2004 Feb;23(2):147-159. doi: 10.1002/humu.10310. Hum Mutat. 2004. PMID: 14722918

5

Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome.

Frints SG, Froyen G, Marynen P, Willekens D, Legius E, Fryns JP. Frints SG, et al. Am J Med Genet. 2002 Nov 1;112(4):427-8. doi: 10.1002/ajmg.10628. Am J Med Genet. 2002. PMID: 12376949 No abstract available.

6

Clinical study and haplotype analysis in two brothers with Partington syndrome.

Frints SG, Borghgraef M, Froyen G, Marynen P, Fryns JP. Frints SG, et al. Am J Med Genet. 2002 Nov 1;112(4):361-8. doi: 10.1002/ajmg.10630. Am J Med Genet. 2002. PMID: 12376938

7

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.

Bienvenu T, Poirier K, Friocourt G, Bahi N, Beaumont D, Fauchereau F, Ben Jeema L, Zemni R, Vinet MC, Francis F, Couvert P, Gomot M, Moraine C, van Bokhoven H, Kalscheuer V, Frints S, Gecz J, Ohzaki K, Chaabouni H, Fryns JP, Desportes V, Beldjord C, Chelly J. Bienvenu T, et al. Hum Mol Genet. 2002 Apr 15;11(8):981-91. doi: 10.1093/hmg/11.8.981. Hum Mol Genet. 2002. PMID: 11971879

8

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.

Strømme P, Mangelsdorf ME, Shaw MA, Lower KM, Lewis SM, Bruyere H, Lütcherath V, Gedeon AK, Wallace RH, Scheffer IE, Turner G, Partington M, Frints SG, Fryns JP, Sutherland GR, Mulley JC, Gécz J. Strømme P, et al. Nat Genet. 2002 Apr;30(4):441-5. doi: 10.1038/ng862. Epub 2002 Mar 11. Nat Genet. 2002. PMID: 11889467

9

Linkage analysis in three families with nonspecific X-linked mental retardation.

Claes S, Gu XX, Legius E, Lorenzetti E, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Claes S, et al. Am J Med Genet. 1996 Jul 12;64(1):137-46. doi: 10.1002/(SICI)1096-8628(19960712)64:1<137::AID-AJMG24>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8826464

10

X-linked mental retardation with dystonic movements of the hands.

Partington MW, Mulley JC, Sutherland GR, Hockey A, Thode A, Turner G. Partington MW, et al. Am J Med Genet. 1988 May-Jun;30(1-2):251-62. doi: 10.1002/ajmg.1320300127. Am J Med Genet. 1988. PMID: 3177452

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