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.
113 related articles for article (PubMed ID: 8237919)
41. A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene. Lachiewicz AM; Spiridigliozzi GA; McConkie-Rosell A; Burgess D; Feng Y; Warren ST; Tarleton J Am J Med Genet; 1996 Aug; 64(2):278-82. PubMed ID: 8844065 [TBL] [Abstract][Full Text] [Related]
42. Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers. Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; Treitman TM Optom Vis Sci; 2000 Nov; 77(11):592-9. PubMed ID: 11138833 [TBL] [Abstract][Full Text] [Related]
44. Diagnostic, carrier and prenatal genetic testing for fragile X syndrome and other FMR-1-related disorders in Johannesburg, South Africa: a 20-year review. Essop FB; Krause A S Afr Med J; 2013 Oct; 103(12 Suppl 1):994-8. PubMed ID: 24300646 [TBL] [Abstract][Full Text] [Related]
45. Symptoms of schizotypal personality disorder in fragile X women. Sobesky WE; Hull CE; Hagerman RJ J Am Acad Child Adolesc Psychiatry; 1994 Feb; 33(2):247-55. PubMed ID: 8150797 [TBL] [Abstract][Full Text] [Related]
46. Molecular-clinical correlations in males with an expanded FMR1 mutation. Merenstein SA; Sobesky WE; Taylor AK; Riddle JE; Tran HX; Hagerman RJ Am J Med Genet; 1996 Aug; 64(2):388-94. PubMed ID: 8844089 [TBL] [Abstract][Full Text] [Related]
47. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing. Ardui S; Race V; Zablotskaya A; Hestand MS; Van Esch H; Devriendt K; Matthijs G; Vermeesch JR Hum Mutat; 2017 Mar; 38(3):324-331. PubMed ID: 27883256 [TBL] [Abstract][Full Text] [Related]
51. Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data. Hamel BC; Smits AP; de Graaff E; Smeets DF; Schoute F; Eussen BH; Knight SJ; Davies KE; Assman-Hulsmans CF; Oostra BA Am J Hum Genet; 1994 Nov; 55(5):923-31. PubMed ID: 7977354 [TBL] [Abstract][Full Text] [Related]
52. Advances in molecular analysis of fragile X syndrome. Warren ST; Nelson DL JAMA; 1994 Feb; 271(7):536-42. PubMed ID: 8301769 [TBL] [Abstract][Full Text] [Related]
53. 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]
54. Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males. Birch RC; Hocking DR; Cornish KM; Menant JC; Georgiou-Karistianis N; Godler DE; Wen W; Hackett A; Rogers C; Trollor JN Genes Brain Behav; 2015 Mar; 14(3):251-9. PubMed ID: 25689687 [TBL] [Abstract][Full Text] [Related]
55. FMR1 gene deletion/reversion: a pitfall of fragile X carrier testing. Gasteiger M; Grasbon-Frodl E; Neitzel B; Kooy F; Holinski-Feder E Genet Test; 2003; 7(4):303-8. PubMed ID: 15000806 [TBL] [Abstract][Full Text] [Related]
56. The Fragile X premutation: new insights and clinical consequences. Van Esch H Eur J Med Genet; 2006; 49(1):1-8. PubMed ID: 16473304 [TBL] [Abstract][Full Text] [Related]
57. [Detection of FMR-1 gene expression by RT-PCR]. Zheng L; Fan Y; Huang T; Zhu N; Shen Y; Wu G Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Dec; 17(6):407-11. PubMed ID: 9208564 [TBL] [Abstract][Full Text] [Related]
58. Amygdala dysfunction in men with the fragile X premutation. Hessl D; Rivera S; Koldewyn K; Cordeiro L; Adams J; Tassone F; Hagerman PJ; Hagerman RJ Brain; 2007 Feb; 130(Pt 2):404-16. PubMed ID: 17166860 [TBL] [Abstract][Full Text] [Related]
59. DNA methylation represses FMR-1 transcription in fragile X syndrome. Sutcliffe JS; Nelson DL; Zhang F; Pieretti M; Caskey CT; Saxe D; Warren ST Hum Mol Genet; 1992 Sep; 1(6):397-400. PubMed ID: 1301913 [TBL] [Abstract][Full Text] [Related]
60. A point mutation in the FMR-1 gene associated with fragile X mental retardation. De Boulle K; Verkerk AJ; Reyniers E; Vits L; Hendrickx J; Van Roy B; Van den Bos F; de Graaff E; Oostra BA; Willems PJ Nat Genet; 1993 Jan; 3(1):31-5. PubMed ID: 8490650 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]