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Journal Abstract Search

189 related items for PubMed ID: 12661811

  • 1.
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  • 2. Clinical and cytogenetic survey of institutionalized mentally retarded patients with emphasis on the fragile-X syndrome.
    Butler MG, Singh DN.
    J Intellect Disabil Res; 1993 Apr; 37 ( Pt 2)(Pt 2):131-42. PubMed ID: 8481611
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  • 3. Fragile X syndrome among children with mental retardation.
    Elango R, Verma IC.
    Indian J Pediatr; 1996 Apr; 63(4):533-8. PubMed ID: 10832474
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  • 4. Syndromes and disorders associated with mental retardation.
    Greydanus DE, Pratt HD.
    Indian J Pediatr; 2005 Oct; 72(10):859-64. PubMed ID: 16272659
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  • 5. Mental retardation.
    Palmer FB, Capute AJ.
    Pediatr Rev; 1994 Dec; 15(12):473-9. PubMed ID: 7845869
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  • 8. Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour.
    Stoyanova M, Hachmeriyan M, Levkova M, Bichev S, Georgieva M, Mladenov V, Angelova L.
    Folia Med (Plovdiv); 2022 Feb 28; 64(1):27-32. PubMed ID: 35851904
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  • 10. Molecular diagnosis of Fragile X syndrome in subjects with intellectual disability of unknown origin: implications of its prevalence in regional Pakistan.
    Kanwal M, Alyas S, Afzal M, Mansoor A, Abbasi R, Tassone F, Malik S, Mazhar K.
    PLoS One; 2015 Feb 28; 10(4):e0122213. PubMed ID: 25875842
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  • 12. Problems in the diagnosis of fragile X syndrome in young children are still present.
    Stoll C.
    Am J Med Genet; 2001 Apr 22; 100(2):110-5. PubMed ID: 11298371
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  • 13. Practitioner review: physical investigations in mental retardation.
    Gillberg C.
    J Child Psychol Psychiatry; 1997 Nov 22; 38(8):889-97. PubMed ID: 9413789
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  • 15. Diagnostic yield of the comprehensive assessment of developmental delay/mental retardation in an institute of child neuropsychiatry.
    Battaglia A, Bianchini E, Carey JC.
    Am J Med Genet; 1999 Jan 01; 82(1):60-6. PubMed ID: 9916845
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  • 19. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK, Gustavson KH, Holmgren G, Nordenson I, Pålsson-Stråe U.
    Clin Genet; 1983 Dec 01; 24(6):393-8. PubMed ID: 6652951
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