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.
6. XLMR genes: update 1994. Neri G; Chiurazzi P; Arena JF; Lubs HA Am J Med Genet; 1994 Jul; 51(4):542-9. PubMed ID: 7943038 [TBL] [Abstract][Full Text] [Related]
7. A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Zemni R; Bienvenu T; Vinet MC; Sefiani A; Carrié A; Billuart P; McDonell N; Couvert P; Francis F; Chafey P; Fauchereau F; Friocourt G; des Portes V; Cardona A; Frints S; Meindl A; Brandau O; Ronce N; Moraine C; van Bokhoven H; Ropers HH; Sudbrak R; Kahn A; Fryns JP; Beldjord C; Chelly J Nat Genet; 2000 Feb; 24(2):167-70. PubMed ID: 10655063 [TBL] [Abstract][Full Text] [Related]
8. Splitting and lumping in the nosology of XLMR. Stevenson RE Am J Med Genet; 2000; 97(3):174-82. PubMed ID: 11449485 [TBL] [Abstract][Full Text] [Related]
9. Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3. Kleefstra T; Yntema HG; Oudakker AR; de Vries BB; van Bokhoven H; Hamel BC; Poppelaars FA; Ausems MG Am J Med Genet; 2002 Jul; 110(4):410-1. PubMed ID: 12116222 [No Abstract] [Full Text] [Related]
10. A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3. Uyguner O; Kayserili H; Li Y; Karaman B; Nürnberg G; Hennies H; Becker C; Nürnberg P; Başaran S; Apak MY; Wollnik B Clin Genet; 2007 Mar; 71(3):212-9. PubMed ID: 17309643 [TBL] [Abstract][Full Text] [Related]
11. Study of X-linked mental retardation (XLMR): summary of 61 families in the Miami/Greenwood Study. Lubs HA; Schwartz CE; Stevenson RE; Arena JF Am J Med Genet; 1996 Jul; 64(1):169-75. PubMed ID: 8826469 [TBL] [Abstract][Full Text] [Related]
12. Sixty years of X-linked mental retardation: a historical footnote. Neri G; Opitz JM Am J Med Genet; 2000; 97(3):228-33. PubMed ID: 11449492 [TBL] [Abstract][Full Text] [Related]
13. A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation. Carrié A; Jun L; Bienvenu T; Vinet MC; McDonell N; Couvert P; Zemni R; Cardona A; Van Buggenhout G; Frints S; Hamel B; Moraine C; Ropers HH; Strom T; Howell GR; Whittaker A; Ross MT; Kahn A; Fryns JP; Beldjord C; Marynen P; Chelly J Nat Genet; 1999 Sep; 23(1):25-31. PubMed ID: 10471494 [TBL] [Abstract][Full Text] [Related]
14. Mental retardation and associated neurological dysfunctions in Down syndrome: a consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways. Rachidi M; Lopes C Eur J Paediatr Neurol; 2008 May; 12(3):168-82. PubMed ID: 17933568 [TBL] [Abstract][Full Text] [Related]
15. Molecular basis of X-linked non-specific mental retardation. Pandey UB; Mittal B Indian J Exp Biol; 2004 Jun; 42(6):549-57. PubMed ID: 15260103 [TBL] [Abstract][Full Text] [Related]