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Journal Abstract Search

508 related items for PubMed ID: 18286823

  • 1. 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; 18(4):417-21. PubMed ID: 18286823
    [Abstract] [Full Text] [Related]

  • 2. 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; 65(6):477-82. PubMed ID: 15151506
    [Abstract] [Full Text] [Related]

  • 3. 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
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  • 4. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
    Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG.
    Eur J Hum Genet; 2007 Apr 01; 15(4):432-40. PubMed ID: 17264869
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  • 5. 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]

  • 6. A 45,X sterile male with Yp disguised as 21p.
    Dávalos IP, Rivera H, Vásquez AI, Gutiérrez-Angulo M, Hernández-Vázquez MC, Cortina-Luna FA, Wong-Ley LE, Domínguez-Quezada MG.
    Am J Med Genet; 2002 Aug 01; 111(2):202-4. PubMed ID: 12210351
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  • 8. 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 Aug 01; 10(2):123-32. PubMed ID: 10422004
    [Abstract] [Full Text] [Related]

  • 9. A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation.
    Hickey SE, Thrush DL, Walters-Sen L, Reshmi SC, Astbury C, Gastier-Foster JM, Atkin J.
    Eur J Med Genet; 2013 Sep 01; 56(9):510-4. PubMed ID: 23856564
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 47(3):267-73. PubMed ID: 15337472
    [Abstract] [Full Text] [Related]

  • 11. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):813-20. PubMed ID: 3688019
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  • 12. 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
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  • 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. Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia.
    Ben-Abdallah-Bouhjar I, Hannachi H, Labalme A, Gmidène A, Mougou S, Soyah N, Gribaa M, Sanlaville D, Elghezal H, Saad A.
    Eur J Med Genet; 2012 Dec 01; 55(8-9):461-5. PubMed ID: 22683462
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  • 17. [Prader-Willi syndrome associated with chromosomal aberration: report of a case].
    Kokura K, Shima H, Mori Y, Ikoma F, Sakamoto H, Furuyama J.
    Hinyokika Kiyo; 1992 Sep 01; 38(9):1079-82. PubMed ID: 1357945
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  • 19. [High-resolution cytogenetic study of a patient with Prader-Willi syndrome].
    Shi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Jun 01; 15(3):217-20. PubMed ID: 8222009
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  • 20. [A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)].
    Lejeune J, Maunoury C, Prieur M, Van den Akker J.
    Ann Genet; 1979 Jun 01; 22(4):210-3. PubMed ID: 317782
    [Abstract] [Full Text] [Related]

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