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PUBMED FOR HANDHELDS

Journal Abstract Search

903 related items for PubMed ID: 19239081

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  • 2. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
    Harvard C, Malenfant P, Koochek M, Creighton S, Mickelson EC, Holden JJ, Lewis ME, Rajcan-Separovic E.
    Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
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  • 5. Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.
    Fang JS, Lee KF, Huang CT, Syu CL, Yang KJ, Wang LH, Liao DL, Chen CH.
    Clin Genet; 2008 Jun; 73(6):585-90. PubMed ID: 18400035
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  • 9. Variability in a family with an insertion involving 5p.
    Marinescu RC, Mamunes P, Kline AD, Schmidt J, Rojas K, Overhauser J.
    Am J Med Genet; 1999 Sep 17; 86(3):258-63. PubMed ID: 10482876
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  • 10. A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis.
    Cornish KM, Cross G, Green A, Willatt L, Bradshaw JM.
    J Med Genet; 1999 Jul 17; 36(7):567-70. PubMed ID: 10424821
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  • 11. Parental origin of chromosome 5 deletions in the cri-du-chat syndrome.
    Overhauser J, McMahon J, Oberlender S, Carlin ME, Niebuhr E, Wasmuth JJ, Lee-Chen J.
    Am J Med Genet; 1990 Sep 17; 37(1):83-6. PubMed ID: 1978567
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  • 12. A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.
    Posmyk R, Panasiuk B, Yatsenko SA, Stankiewicz P, Midro AT.
    Genet Couns; 2005 Sep 17; 16(1):17-25. PubMed ID: 15844774
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  • 17. Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion.
    Vialard F, Robyr R, Hillion Y, Molina Gomes D, Selva J, Ville Y.
    Prenat Diagn; 2005 Apr 17; 25(4):311-3. PubMed ID: 15849798
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  • 19. Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3).
    Hodge JC, Lawson-Yuen A, Stoler JM, Ligon AH.
    Cytogenet Genome Res; 2007 Apr 17; 119(1-2):15-20. PubMed ID: 18160776
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