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Journal Abstract Search

447 related items for PubMed ID: 9715326

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  • 6. 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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  • 7. 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 Jul; 19(4):381-6. PubMed ID: 19239081
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  • 9. Cri-du-chat.
    Sigafoos J, O'Reilly MF, Lancioni GE.
    Dev Neurorehabil; 2009 Jun; 12(3):119-21. PubMed ID: 19466618
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  • 10. 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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  • 12. [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 Sep; 45(1):95-7. PubMed ID: 14666800
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  • 14. A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome.
    Elmakky A, Carli D, Lugli L, Torelli P, Guidi B, Falcinelli C, Fini S, Ferrari F, Percesepe A.
    Eur J Med Genet; 2014 Mar; 57(4):145-50. PubMed ID: 24556499
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  • 15. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.
    Petit P, Fryns JP.
    Genet Couns; 1990 Mar; 1(2):179-84. PubMed ID: 2081002
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  • 16. Cri-du-chat syndrome.
    Chang CY, Lin SP, Lin HY, Chen YJ, Kao HA, Yeung CY, Hsu CH, Chi H.
    Acta Paediatr Taiwan; 2007 Mar; 48(6):328-31. PubMed ID: 18437967
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  • 17. Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR.
    Wu Q, Niebuhr E, Yang H, Hansen L.
    Eur J Hum Genet; 2005 Apr; 13(4):475-85. PubMed ID: 15657623
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  • 18. 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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