These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
267 related articles for article (PubMed ID: 15319782)
1. Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations. Mandel JL; Chelly J Eur J Hum Genet; 2004 Sep; 12(9):689-93. PubMed ID: 15319782 [TBL] [Abstract][Full Text] [Related]
2. [ARX mutations and mental retardation of unknown etiology: three new cases in Spain]. Romero-Rubio MT; Andrés-Celma M; Castelló-Pomares ML; Roselló M; Ferrer-Bolufer I; Martínez-Castellano F Rev Neurol; 2008 Dec 16-31; 47(12):634-7. PubMed ID: 19085879 [TBL] [Abstract][Full Text] [Related]
3. A novel mutation of the ARX gene in a male with nonsyndromic mental retardation. Troester MM; Trachtenberg T; Narayanan V J Child Neurol; 2007 Jun; 22(6):744-8. PubMed ID: 17641262 [TBL] [Abstract][Full Text] [Related]
4. XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene. Stepp ML; Cason AL; Finnis M; Mangelsdorf M; Holinski-Feder E; Macgregor D; MacMillan A; Holden JJ; Gecz J; Stevenson RE; Schwartz CE BMC Med Genet; 2005 Apr; 6():16. PubMed ID: 15850492 [TBL] [Abstract][Full Text] [Related]
5. Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand. Rujirabanjerd S; Tongsippunyoo K; Sripo T; Limprasert P Eur J Med Genet; 2007; 50(5):346-54. PubMed ID: 17613295 [TBL] [Abstract][Full Text] [Related]
6. ARX mutation c.428-451dup (24bp) in a Brazilian family with X-linked mental retardation. Gestinari-Duarte Rde S; Santos-Rebouças CB; Boy RT; Pimentel MM Eur J Med Genet; 2006; 49(3):269-75. PubMed ID: 16762829 [TBL] [Abstract][Full Text] [Related]
9. ARX: a gene for all seasons. Gécz J; Cloosterman D; Partington M Curr Opin Genet Dev; 2006 Jun; 16(3):308-16. PubMed ID: 16650978 [TBL] [Abstract][Full Text] [Related]
10. Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation. Turner G; Partington M; Kerr B; Mangelsdorf M; Gecz J Am J Med Genet; 2002 Nov; 112(4):405-11. PubMed ID: 12376946 [TBL] [Abstract][Full Text] [Related]
17. Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons. Colombo E; Galli R; Cossu G; Gécz J; Broccoli V Dev Dyn; 2004 Nov; 231(3):631-9. PubMed ID: 15376319 [TBL] [Abstract][Full Text] [Related]
18. The function of the Aristaless-related homeobox (Arx) gene product as a transcriptional repressor is diminished by mutations associated with X-linked mental retardation (XLMR). Fullenkamp AN; El-Hodiri HM Biochem Biophys Res Commun; 2008 Dec; 377(1):73-8. PubMed ID: 18835247 [TBL] [Abstract][Full Text] [Related]
19. Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis. Poirier K; Lacombe D; Gilbert-Dussardier B; Raynaud M; Desportes V; de Brouwer AP; Moraine C; Fryns JP; Ropers HH; Beldjord C; Chelly J; Bienvenu T Neurogenetics; 2006 Mar; 7(1):39-46. PubMed ID: 16235064 [TBL] [Abstract][Full Text] [Related]
20. Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium. de Brouwer AP; Yntema HG; Kleefstra T; Lugtenberg D; Oudakker AR; de Vries BB; van Bokhoven H; Van Esch H; Frints SG; Froyen G; Fryns JP; Raynaud M; Moizard MP; Ronce N; Bensalem A; Moraine C; Poirier K; Castelnau L; Saillour Y; Bienvenu T; Beldjord C; des Portes V; Chelly J; Turner G; Fullston T; Gecz J; Kuss AW; Tzschach A; Jensen LR; Lenzner S; Kalscheuer VM; Ropers HH; Hamel BC Hum Mutat; 2007 Feb; 28(2):207-8. PubMed ID: 17221867 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]