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Journal Abstract Search

245 related items for PubMed ID: 19466618

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  • 5. 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; 37(1):83-6. PubMed ID: 1978567
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  • 7. Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
    Laczmanska I, Stembalska A, Gil J, Czemarmazowicz H, Sasiadek M.
    Eur J Med Genet; 2006 Sep; 49(1):87-92. PubMed ID: 16473315
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  • 8. Narrative discourse and sociocognitive abilities of a child with Cri-du-Chat syndrome.
    Albano S, Piccardi L, Pizzamiglio MR, Volpe C, D'Amico S.
    J Genet Psychol; 2013 Sep; 174(1):51-72. PubMed ID: 23534097
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  • 9. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D, Boccone L, Ristaldi MS, Nucaro AL.
    Genet Couns; 2008 Sep; 19(4):381-6. PubMed ID: 19239081
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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; 36(7):567-70. PubMed ID: 10424821
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  • 12. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.
    Benn PA, Hsu LY, Verma RS, Alonso ML, Reich E, Wishnick M.
    Obstet Gynecol; 1987 Sep; 70(3 Pt 2):449-52. PubMed ID: 3627600
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  • 13. Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes.
    Clarke DJ, Boer H.
    Am J Ment Retard; 1998 Nov; 103(3):264-71. PubMed ID: 9833657
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  • 15. Cri-du-chat syndrome diagnosed by amniocentesis performed due to abnormal maternal serum test.
    Fankhauser L, Brundler AM, Dahoun S.
    Prenat Diagn; 1998 Oct; 18(10):1099-100. PubMed ID: 9826907
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  • 16. Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines.
    Kitsiou S, Kolialexi A, Mavrou A.
    Prenat Diagn; 2004 Jul; 24(7):578-9. PubMed ID: 15300755
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  • 17. Ocular findings in a patient with deletion short arm chromosome 5 (cri du chat) and ring chromosome 14.
    Clark DI, Howard PJ, Patterson A.
    Trans Ophthalmol Soc U K (1962); 1986 Jul; 105 ( Pt 6)():723-5. PubMed ID: 3477901
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  • 19. [Cri-du-chat syndrome. A case report].
    Diop IB, Sy Signate H, Ba SA, Sarr M, Hane L, Diame H, Kane A, Dieye O, Sow D, Diouf SM, Fall M.
    Dakar Med; 2000 Jul; 45(1):95-7. PubMed ID: 14666800
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