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Journal Abstract Search

282 related items for PubMed ID: 8160287

  • 1. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G, Tükün A, Yalaz K, Bökesoy I.
    Turk J Pediatr; 1993; 35(4):333-6. PubMed ID: 8160287
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  • 2. [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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  • 7. 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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  • 9. Unique karyotypes in two patients with Prader-Willi syndrome.
    Narahara K, Hiramoto K, Murakami M, Miyake S, Tsuji K, Yokoyama Y, Namba H, Ninomiya S, Murakami R, Seino Y.
    Am J Med Genet; 1992 Mar 01; 42(5):671-7. PubMed ID: 1632436
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  • 14. Use of FISH technique in the diagnosis of chromosomal syndromes.
    Iqbal MA, Ulmer C, Sakati N.
    East Mediterr Health J; 1999 Nov 01; 5(6):1218-24. PubMed ID: 11924115
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  • 15. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
    Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):791-802. PubMed ID: 3688017
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  • 20. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP.
    Genet Couns; 1999 Dec 01; 10(2):123-32. PubMed ID: 10422004
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