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.
3. A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse. Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP Genes Brain Behav; 2004 Dec; 3(6):337-59. PubMed ID: 15544577 [TBL] [Abstract][Full Text] [Related]
4. Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3). Balci S; Unal A; Engiz O; Aktas D; Liehr T; Gross M; Mrasek K; Saygi S Dev Med Child Neurol; 2007 Mar; 49(3):219-24. PubMed ID: 17355480 [TBL] [Abstract][Full Text] [Related]
5. [Genetics of mental retardation]. Prieto García F Neurologia; 1998 May; 13(5):218-22. PubMed ID: 9646628 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology. Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; Koukoulli R; Anastasiadou V; Deltas CC; Middleton L Genet Couns; 1997; 8(1):1-6. PubMed ID: 9101271 [TBL] [Abstract][Full Text] [Related]
8. Screening for fragile X syndrome. Murray J; Cuckle H; Taylor G; Hewison J Health Technol Assess; 1997; 1(4):i-iv, 1-71. PubMed ID: 9414543 [TBL] [Abstract][Full Text] [Related]
9. The emerging genetic theories of unstable DNA, uniparental disomy, and imprinting. Wilkins-Haug L Curr Opin Obstet Gynecol; 1993 Apr; 5(2):179-85. PubMed ID: 8490087 [TBL] [Abstract][Full Text] [Related]
10. Clinical variability of the 22q11.2 duplication syndrome. Wentzel C; Fernström M; Ohrner Y; Annerén G; Thuresson AC Eur J Med Genet; 2008; 51(6):501-10. PubMed ID: 18707033 [TBL] [Abstract][Full Text] [Related]
11. The frequency of fragile X syndrome among selected patients at Songklanagarind Hospital during 1991-1996, studied by cytogenetic and molecular methods. Jinorose U; Vasiknanonte P; Limprasert P; Brown WT; Panich V Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():69-74. PubMed ID: 9640603 [TBL] [Abstract][Full Text] [Related]
12. Compound heterozygous female with fragile X syndrome. Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; Taylor AK Am J Med Genet; 1999 Apr; 83(4):318-21. PubMed ID: 10208169 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review. De Smedt B; Swillen A; Verschaffel L; Ghesquière P Dev Disabil Res Rev; 2009; 15(1):4-10. PubMed ID: 19213009 [TBL] [Abstract][Full Text] [Related]
15. Fragile X-syndrome: literature review and report of two cases. Ridaura-Ruiz L; Quinteros-Borgarello M; Berini-Aytés L; Gay-Escoda C Med Oral Patol Oral Cir Bucal; 2009 Sep; 14(9):e434-9. PubMed ID: 19718005 [TBL] [Abstract][Full Text] [Related]
19. Expression of fragile Xq 27.3 in a patient with clinical features of deletion 9p syndrome. Kar B Indian Pediatr; 1995 Jul; 32(7):801-3. PubMed ID: 8617559 [No Abstract] [Full Text] [Related]
20. Scope for more genetic testing in learning disability. Case report of an inherited duplication on the X-chromosome. Robertshaw BA; MacPherson J Br J Psychiatry; 2006 Aug; 189():99-101. PubMed ID: 16880477 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]