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24. Neuro-cognitive and behavioural aspects in non-specific mental retardation. A proposal for phenotyping new XLMR genes. Borghgraef M; Sacco S; Gomot M; De Vos B; Jacobs A; Buret V; Desportes V Genet Couns; 2002; 13(2):195-8. PubMed ID: 12150223 [No Abstract] [Full Text] [Related]
26. False conclusions about Vineland standard scores: Silverstein's type I errors and other artifacts. Cicchetti DV; Sparrow SS Am J Ment Defic; 1986 Jul; 91(1):5-9. PubMed ID: 3740116 [TBL] [Abstract][Full Text] [Related]
27. X-linked mental retardation: many genes for a complex disorder. Ropers HH Curr Opin Genet Dev; 2006 Jun; 16(3):260-9. PubMed ID: 16647850 [TBL] [Abstract][Full Text] [Related]
28. X-linked mental retardation: further lumping, splitting and emerging phenotypes. Kleefstra T; Hamel BC Clin Genet; 2005 Jun; 67(6):451-67. PubMed ID: 15857409 [TBL] [Abstract][Full Text] [Related]
29. 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]
31. Clinical variables at age 2 predictive of mental retardation at age 5 in children with pervasive developmental disorder. Takeda T; Koyama T; Kanai C; Kurita H Psychiatry Clin Neurosci; 2005 Dec; 59(6):717-22. PubMed ID: 16401249 [TBL] [Abstract][Full Text] [Related]
32. No "fragile X" chromosome in normal men. Soudek D; Gornzy N Clin Genet; 1981 Feb; 19(2):140-1. PubMed ID: 7471510 [No Abstract] [Full Text] [Related]
33. Cognitive, language, and adaptive behavior profiles in individuals with a diagnosis of Cohen syndrome. Karpf J; Turk J; Howlin P Clin Genet; 2004 Apr; 65(4):327-32. PubMed ID: 15025727 [TBL] [Abstract][Full Text] [Related]
34. In search of the MRX genes. Toniolo D Am J Med Genet; 2000; 97(3):221-7. PubMed ID: 11449491 [TBL] [Abstract][Full Text] [Related]
35. The fragile X chromosome mental retardation and large testes. Hecht F; Kaiser-McCaw B; Moore BC; Cadien J; Glover TW Ariz Med; 1980 Nov; 37(11):764-6. PubMed ID: 7224864 [No Abstract] [Full Text] [Related]
36. Fragile X syndrome a case report of a family. Chatterjee C; Guha D; Das S; Singh SK; Dasgupta U; Saha S; Bannerjee D Indian J Pathol Microbiol; 2001 Oct; 44(4):499-502. PubMed ID: 12035381 [TBL] [Abstract][Full Text] [Related]
37. The capacity to consent to treatment and research: a review of standardized assessment tools. Sturman ED Clin Psychol Rev; 2005 Nov; 25(7):954-74. PubMed ID: 15964671 [TBL] [Abstract][Full Text] [Related]
38. Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH. Kousoulidou L; Parkel S; Zilina O; Palta P; Puusepp H; Remm M; Turner G; Boyle J; van Bokhoven H; de Brouwer A; Van Esch H; Froyen G; Ropers HH; Chelly J; Moraine C; Gecz J; Kurg A; Patsalis PC Eur J Med Genet; 2007; 50(6):399-410. PubMed ID: 17980689 [TBL] [Abstract][Full Text] [Related]
39. Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation. Kutsche K; Yntema H; Brandt A; Jantke I; Nothwang HG; Orth U; Boavida MG; David D; Chelly J; Fryns JP; Moraine C; Ropers HH; Hamel BC; van Bokhoven H; Gal A Nat Genet; 2000 Oct; 26(2):247-50. PubMed ID: 11017088 [TBL] [Abstract][Full Text] [Related]
40. [Current concepts of X-linked myopathies and social consequences of their diagnosis (apropos of 88 cases)]. Serratrice G; Cros D; Pellissier JF; Pouget J Bull Acad Natl Med; 1981 Dec; 165(9):1229-41. PubMed ID: 7044494 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]