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Journal Abstract Search

561 related items for PubMed ID: 25691410

  • 21. [Phenotype-genotype correlation analysis of 12 cases with Angelman/Prader-Willi syndrome].
    Chen C, Peng Y, Xia Y, Li H, Zhu H, Pan Q, Yin F, Wu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):708-12. PubMed ID: 25449072
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  • 22. [From the clinical to the genetic diagnosis of Prader-Willi and Angelman syndromes].
    Camprubí-Sánchez C, Gabau-Vila E, Artigas-Pallarés J, Coll-Sandiumenge MD, Guitart-Feliubadaló M.
    Rev Neurol; 2006 Jan 07; 42 Suppl 1():S61-7. PubMed ID: 16506135
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  • 23. 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
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  • 26. A Comparative Study of Sociability in Angelman, Cornelia de Lange, Fragile X, Down and Rubinstein Taybi Syndromes and Autism Spectrum Disorder.
    Moss J, Nelson L, Powis L, Waite J, Richards C, Oliver C.
    Am J Intellect Dev Disabil; 2016 Nov 13; 121(6):465-486. PubMed ID: 27802104
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  • 28. The prevalence and phenomenology of repetitive behavior in genetic syndromes.
    Moss J, Oliver C, Arron K, Burbidge C, Berg K.
    J Autism Dev Disord; 2009 Apr 13; 39(4):572-88. PubMed ID: 19037716
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  • 29. Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.
    White HE, Hall VJ, Cross NC.
    Clin Chem; 2007 Nov 13; 53(11):1960-2. PubMed ID: 17890436
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  • 30. Evaluation of an In-House Genetic Testing Method for Confirming Prader-Willi and Angelman Syndromes in Sri Lanka.
    Kugalingam N, Silva D, Rathnayake P, Atapattu N, Ranaweera DM, Chandrasekharan NV.
    Clin Lab; 2024 Aug 01; 70(8):. PubMed ID: 39193956
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  • 31. Angelman syndrome assessed by neurological and molecular cytogenetic investigations.
    Hou JW, Wang PJ, Wang TR.
    Pediatr Neurol; 1997 Jan 01; 16(1):17-22. PubMed ID: 9044396
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  • 32. Prader-Willi syndrome and Angelman syndrome.
    Buiting K.
    Am J Med Genet C Semin Med Genet; 2010 Aug 15; 154C(3):365-76. PubMed ID: 20803659
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  • 35. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
    Zeschnigk M, Schmitz B, Dittrich B, Buiting K, Horsthemke B, Doerfler W.
    Hum Mol Genet; 1997 Mar 15; 6(3):387-95. PubMed ID: 9147641
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  • 37. Referral diagnosis of Prader-Willi syndrome and Angelman syndrome based on methylation-specific polymerase chain reaction.
    Teng YN, Tsai WH, Wu CJ, Lin SJ, Chen YJ, Kuo PL.
    J Formos Med Assoc; 2002 Jul 15; 101(7):488-94. PubMed ID: 12353341
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  • 38. Variance in the pathophysiological impact of the hemizygosity of gamma-aminobutyric acid type A receptor subunit genes between Prader-Willi syndrome and Angelman syndrome.
    Egawa K, Saitoh S, Asahina N, Shiraishi H.
    Brain Dev; 2021 Apr 15; 43(4):521-527. PubMed ID: 33419637
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  • 39. Genetic testing for Prader-Willi and Angelman syndromes.
    Schad CR, Jalal SM, Thibodeau SN.
    Mayo Clin Proc; 1995 Dec 15; 70(12):1195-6. PubMed ID: 7490922
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  • 40. A genetic model for the Prader-Willi syndrome and its implication for Angelman syndrome.
    Kennerknecht I.
    Hum Genet; 1992 Dec 15; 90(1-2):91-8. PubMed ID: 1427794
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