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Journal Abstract Search

310 related items for PubMed ID: 23856564

  • 1. 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; 56(9):510-4. PubMed ID: 23856564
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  • 2. 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; 47(3):267-73. PubMed ID: 15337472
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  • 5. Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3).
    Dang V, Surampalli A, Manzardo AM, Youn S, Butler MG, Gold JA, Kimonis VE.
    Cytogenet Genome Res; 2016 Sep; 150(1):29-34. PubMed ID: 27894106
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  • 6. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
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  • 8. Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: report and a review of literature.
    Liu AP, Tang WF, Lau ET, Chan KY, Kan AS, Wong KY, Tso WW, Jalal K, Lee SL, Chau CS, Chung BH.
    Am J Med Genet A; 2013 Jun; 161A(6):1309-18. PubMed ID: 23633107
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  • 9. Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome.
    Rivera H, Zuffardi O, Gargantini L.
    Am J Med Genet; 1990 Nov; 37(3):311-7. PubMed ID: 2260556
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  • 10. 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; 15(4):432-40. PubMed ID: 17264869
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  • 11. 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 Apr; 18(4):417-21. PubMed ID: 18286823
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  • 16. Prader-Willi syndrome.
    Cassidy SB, Ledbetter DH.
    Neurol Clin; 1989 Feb; 7(1):37-54. PubMed ID: 2646521
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  • 18. 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
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  • 19. Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes.
    Jauch A, Robson L, Smith A.
    Hum Genet; 1995 Sep 30; 96(3):345-9. PubMed ID: 7649555
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  • 20. 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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