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Journal Abstract Search

345 related items for PubMed ID: 16190961

  • 1. Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome.
    Ninomiya S, Yokoyama Y, Kawakami M, Une T, Maruyama H, Morishima T.
    Pediatr Int; 2005 Oct; 47(5):541-5. PubMed ID: 16190961
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  • 2. [Prader-Willi syndrome and genomic imprinting].
    Wang W, Wang DF, Cui YF, Ni JH, Dong ZY, Fu MF, Fu HM, Lu GQ, Chen FS.
    Zhonghua Er Ke Za Zhi; 2003 Jun; 41(6):453-6. PubMed ID: 14749005
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  • 3. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M, Portis T, Longnecker R, Nicholls RD.
    Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
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  • 6. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
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  • 9. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.
    Jiang YH, Wauki K, Liu Q, Bressler J, Pan Y, Kashork CD, Shaffer LG, Beaudet AL.
    BMC Genomics; 2008 Jan 28; 9():50. PubMed ID: 18226259
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  • 10. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
    Hassan M, Butler MG.
    Eur J Med Genet; 2016 Nov 28; 59(11):584-589. PubMed ID: 27659713
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  • 13. Prader-Willi syndrome: reflections on seminal studies and future therapies.
    Chung MS, Langouët M, Chamberlain SJ, Carmichael GG.
    Open Biol; 2020 Sep 28; 10(9):200195. PubMed ID: 32961075
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  • 14. 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 28; 47(3):267-73. PubMed ID: 15337472
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  • 15. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC, Person RE, Flores A, Villanos MT, Bi W, Wiszniewska J, Bacino CA.
    Am J Med Genet A; 2012 Oct 28; 158A(10):2557-63. PubMed ID: 22903639
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  • 18. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.
    Zilina O, Kahre T, Talvik I, Oiglane-Shlik E, Tillmann V, Ounap K.
    Eur J Med Genet; 2014 Oct 28; 57(6):279-83. PubMed ID: 24704109
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  • 20. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K.
    Acta Paediatr Suppl; 1997 Nov 28; 423():55-7. PubMed ID: 9401540
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