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Journal Abstract Search

321 related items for PubMed ID: 10832474

  • 21. FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardation.
    Mulatinho MV, Llerena JC, Pimentel MM.
    Genet Test; 2000; 4(3):283-7. PubMed ID: 11142760
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  • 23. 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; 50(4):368-76. PubMed ID: 24630283
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  • 24. A step-wise diagnosis of fragile X syndrome in Taiwan.
    Huang YT, Chiang SC, Tzeng CC, Liu CH, Chien YH, Hwu WL.
    Acta Paediatr Taiwan; 2004 Apr; 45(2):69-72. PubMed ID: 15335113
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  • 29. Molecular screening for fragile X syndrome in mentally handicapped children in Korea.
    Kwon SH, Lee KS, Hyun MC, Song KE, Kim JK.
    J Korean Med Sci; 2001 Jun; 16(3):271-5. PubMed ID: 11410685
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  • 32. A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology.
    Bundey S, Webb TP, Thake A, Todd J.
    J Med Genet; 1985 Aug; 22(4):258-66. PubMed ID: 4045951
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  • 35. Population based prenatal screening for the fragile X syndrome.
    Palomaki GE.
    J Med Screen; 1994 Jan; 1(1):65-72. PubMed ID: 8790488
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  • 36. Fragile X mental retardation: prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern.
    Sanfilippo S, Ragusa RM, Musumeci S, Neri G.
    Am J Med Genet; 1986 Jan; 23(1-2):589-95. PubMed ID: 3953669
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  • 38. Population incidence and segregation ratios in the Martin-Bell syndrome.
    Webb TP, Bundey SE, Thake AI, Todd J.
    Am J Med Genet; 1986 Jan; 23(1-2):573-80. PubMed ID: 3953667
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