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Journal Abstract Search

122 related items for PubMed ID: 3791673

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  • 8. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
    Magenis RE, Toth-Fejel S, Allen LJ, Black M, Brown MG, Budden S, Cohen R, Friedman JM, Kalousek D, Zonana J.
    Am J Med Genet; 1990 Mar; 35(3):333-49. PubMed ID: 2309780
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  • 10. [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Götz J, Krüger G, Westphal BC, Pelz L.
    Kinderarztl Prax; 1989 May; 57(5):239-43. PubMed ID: 2747122
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  • 12. Prader-Willi syndrome in two siblings: one with normal karyotype, one with a terminal deletion of distal Xq.
    Ishikawa T, Kanayama M, Wada Y.
    Clin Genet; 1987 Nov; 32(5):295-9. PubMed ID: 3319293
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  • 14. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
    Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ.
    Eur J Paediatr Neurol; 2000 Nov; 4(1):39-43. PubMed ID: 10701104
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  • 16. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
    Qumsiyeh MB, Dalton JD, Gordon PL, Wilroy RS, Tharapel AT.
    Am J Med Genet; 1992 Jan 01; 42(1):109-11. PubMed ID: 1308348
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  • 17. Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.
    Smith A, Prasad M, Deng ZM, Robson L, Woodage T, Trent RJ.
    Arch Dis Child; 1995 May 01; 72(5):397-402. PubMed ID: 7618904
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