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Journal Abstract Search

291 related items for PubMed ID: 1308348

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Derivative Y chromosome resulting from a t(Y;15) (q12;q11.2) in a boy with Prader-Willi syndrome.
    Suzuki Y, Sasagawa I, Sawamura T, Ishigooka M, Kaneko H, Kubota Y, Nakada T.
    Int Urol Nephrol; 1996 Jan 01; 28(6):797-800. PubMed ID: 9089049
    [Abstract] [Full Text] [Related]

  • 3. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
    Cassidy SB, Thuline HC, Holm VA.
    Am J Med Genet; 1984 Feb 01; 17(2):485-95. PubMed ID: 6336316
    [Abstract] [Full Text] [Related]

  • 4. Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).
    Park JP, Moeschler JB, Hani VH, Hawk AB, Belloni DR, Noll WW, Mohandas TK.
    Am J Med Genet; 1998 Jun 30; 78(2):134-9. PubMed ID: 9674903
    [Abstract] [Full Text] [Related]

  • 5. Prader-Willi syndrome.
    Cassidy SB, Ledbetter DH.
    Neurol Clin; 1989 Feb 30; 7(1):37-54. PubMed ID: 2646521
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.
    Toth-Fejel S, Magenis RE, Leff S, Brown MG, Comegys B, Lawce H, Berry T, Kesner D, Webb MJ, Olson S.
    Am J Med Genet; 1995 Feb 13; 55(4):444-52. PubMed ID: 7762584
    [Abstract] [Full Text] [Related]

  • 7. Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.
    Tantravahi U, Nicholls RD, Stroh H, Ringer S, Neve RL, Kaplan L, Wharton R, Wurster-Hill D, Graham JM, Cantú ES.
    Am J Med Genet; 1989 May 13; 33(1):78-87. PubMed ID: 2750788
    [Abstract] [Full Text] [Related]

  • 8. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
    Puvabanditsin S, Garrow E, Razi S, Mohar AG, Tadros JJ, Phattraprayoon N, Patel P.
    Genet Couns; 2007 May 13; 18(4):417-21. PubMed ID: 18286823
    [Abstract] [Full Text] [Related]

  • 9. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA.
    Clin Genet; 2004 Jun 13; 65(6):477-82. PubMed ID: 15151506
    [Abstract] [Full Text] [Related]

  • 10. De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.
    Cuoco C, Bicocchi MP, Granata D, Mezzano P, Serra G.
    Am J Med Genet; 1990 Sep 13; 37(1):62-4. PubMed ID: 2240045
    [Abstract] [Full Text] [Related]

  • 11. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
    Varela MC, Lopes GM, Koiffmann CP.
    Ann Genet; 2004 Sep 13; 47(3):267-73. PubMed ID: 15337472
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
    Wiriyaukaradecha S, Patmasiriwat P, Wasant P, Tantiniti P.
    Southeast Asian J Trop Med Public Health; 2003 Dec 01; 34(4):881-6. PubMed ID: 15115105
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G, Tükün A, Yalaz K, Bökesoy I.
    Turk J Pediatr; 1993 Dec 01; 35(4):333-6. PubMed ID: 8160287
    [Abstract] [Full Text] [Related]

  • 16. True telomeric translocation in a baby with the Prader-Willi phenotype.
    Reeve A, Norman A, Sinclair P, Whittington-Smith R, Hamey Y, Donnai D, Read A.
    Am J Med Genet; 1993 Aug 01; 47(1):1-6. PubMed ID: 8368237
    [Abstract] [Full Text] [Related]

  • 17. The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants.
    Fukushima Y, Niikawa N, Kuroki Y.
    Jinrui Idengaku Zasshi; 1984 Mar 01; 29(1):1-6. PubMed ID: 6748325
    [No Abstract] [Full Text] [Related]

  • 18. [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Götz J, Krüger G, Westphal BC, Pelz L.
    Kinderarztl Prax; 1989 May 01; 57(5):239-43. PubMed ID: 2747122
    [Abstract] [Full Text] [Related]

  • 19. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Kousseff BG, Diamond T, Essig Y, Miller K, Tedesco T.
    Am J Med Genet; 1987 Dec 01; 28(4):803-11. PubMed ID: 3688018
    [Abstract] [Full Text] [Related]

  • 20. Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
    Schwartz S, Max SR, Panny SR, Cohen MM.
    Am J Med Genet; 1985 Feb 01; 20(2):255-63. PubMed ID: 2858158
    [Abstract] [Full Text] [Related]

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