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Journal Abstract Search

119 related items for PubMed ID: 10331591

  • 1. Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology.
    Tunçbilek E, Alikasifoğlu M, Boduroğlu K, Aktas D, Anar B.
    Am J Med Genet; 1999 May 28; 84(3):202-3. PubMed ID: 10331591
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  • 2. Fragile X syndrome among children with mental retardation.
    Elango R, Verma IC.
    Indian J Pediatr; 1996 May 28; 63(4):533-8. PubMed ID: 10832474
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  • 3. 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 May 28; 10(4):e0122213. PubMed ID: 25875842
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  • 4. [Molecular diagnosis of fragile X syndrome].
    Ben Jemaa L, Khemir S, Maazoul F, Richard L, Beldjord C, Chaabouni M, Chaabouni H.
    Tunis Med; 2008 Nov 28; 86(11):973-7. PubMed ID: 19213487
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  • 5. Fragile site X chromosomes in mentally retarded boys.
    Moon HR, Moon SY.
    J Korean Med Sci; 1993 Jun 28; 8(3):192-6. PubMed ID: 8240748
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  • 6. A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome.
    Demirhan O, Taştemir D, Diler RS, Firat S, Avci A.
    Yonsei Med J; 2003 Aug 30; 44(4):583-92. PubMed ID: 12950112
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  • 8. Applicability of a checklist for clinical screening of the fragile X syndrome.
    Arvio M, Peippo M, Simola KO.
    Clin Genet; 1997 Oct 30; 52(4):211-5. PubMed ID: 9383025
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  • 11. Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.
    Gustavson KH, Blomquist HK, Holmgren G.
    Am J Med Genet; 1986 Oct 30; 23(1-2):581-7. PubMed ID: 3953668
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  • 13. Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children.
    Gérard B, Le Heuzey MF, Brunie G, Lewine P, Saiag MC, Cacheux V, Da Silva F, Dugas M, Mouren-Simeoni MC, Elion J, Grandchamp B.
    Ann Genet; 1997 Oct 30; 40(3):139-44. PubMed ID: 9401101
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  • 15. Frequency of the fragile X syndrome in Japanese mentally retarded males.
    Arinami T, Kondo I, Nakajima S.
    Hum Genet; 1986 Aug 30; 73(4):309-12. PubMed ID: 3744362
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  • 18. FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardation.
    Mulatinho MV, Llerena JC, Pimentel MM.
    Genet Test; 2000 Aug 30; 4(3):283-7. PubMed ID: 11142760
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  • 19. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG, Hussein IR, Abuzenadah A, Gari M, Bassiouni R, Sogaty S, Lary S, Al-Quaiti M, Al Balwi M, Al Qahtani M.
    Pediatr Neurol; 2014 Apr 30; 50(4):368-76. PubMed ID: 24630283
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  • 20. Intellectual disability in boys: mark the face!
    Saini S, Singanamala B, Saini AG.
    BMJ Case Rep; 2019 May 09; 12(5):. PubMed ID: 31076495
    [No Abstract] [Full Text] [Related]

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