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Journal Abstract Search

321 related items for PubMed ID: 8910878

  • 21. [Genomic imprinting and its related diseases].
    Niikawa N.
    Tanpakushitsu Kakusan Koso; 1997 Dec; 42(16):2626-32. PubMed ID: 9404158
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  • 23. Clinical and molecular characterization of a large family with an interstitial 15q11q13 duplication.
    Piard J, Philippe C, Marvier M, Beneteau C, Roth V, Valduga M, Béri M, Bonnet C, Grégoire MJ, Jonveaux P, Leheup B.
    Am J Med Genet A; 2010 Aug; 152A(8):1933-41. PubMed ID: 20635369
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  • 26. Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes.
    Nicholls RD.
    Curr Opin Genet Dev; 1993 Jun; 3(3):445-56. PubMed ID: 8353420
    [Abstract] [Full Text] [Related]

  • 27. In and around SNRPN.
    Lalande M.
    Nat Genet; 1994 Sep; 8(1):5-7. PubMed ID: 7987391
    [No Abstract] [Full Text] [Related]

  • 28. Genetics of childhood disorders: XII. Genomic imprinting: breaking the rules.
    Everman DB, Cassidy SB.
    J Am Acad Child Adolesc Psychiatry; 2000 Mar; 39(3):386-9. PubMed ID: 10714060
    [No Abstract] [Full Text] [Related]

  • 29. Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.
    Gurrieri F, Accadia M.
    Endocr Dev; 2009 Mar; 14():20-8. PubMed ID: 19293572
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  • 31. Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns.
    Alshawsh M, Wake M, Gecz J, Corbett M, Saffery R, Pitt J, Greaves R, Williams K, Field M, Cheong J, Bui M, Arora S, Sadedin S, Lunke S, Wall M, Amor DJ, Godler DE.
    Epigenomics; 2024 Mar; 16(18):1203-1214. PubMed ID: 39365098
    [Abstract] [Full Text] [Related]

  • 32. Towards a molecular understanding of Prader-Willi and Angelman syndromes.
    Mann MR, Bartolomei MS.
    Hum Mol Genet; 1999 Mar; 8(10):1867-73. PubMed ID: 10469839
    [Abstract] [Full Text] [Related]

  • 33. [Genomic imprinting and hereditary diseases].
    Orstavik KH.
    Tidsskr Nor Laegeforen; 1999 Feb 28; 119(6):835-8. PubMed ID: 10101947
    [Abstract] [Full Text] [Related]

  • 34. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
    Nicholls RD.
    Am J Med Genet; 1993 Apr 01; 46(1):16-25. PubMed ID: 8388169
    [Abstract] [Full Text] [Related]

  • 35. Analysis of DEXI/Dexi refines the organization of the mouse 7C and human 15q11-->q13 imprinting clusters.
    Kelly M, Edgar AJ, Wevrick R.
    Cytogenet Cell Genet; 2001 Apr 01; 92(1-2):149-52. PubMed ID: 11306815
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  • 38. Competitive edge at the imprinted Prader-Willi/Angelman region?
    Tilghman SM, Caspary T, Ingram RS.
    Nat Genet; 1998 Mar 01; 18(3):206-8. PubMed ID: 9500535
    [No Abstract] [Full Text] [Related]

  • 39. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC, Driscoll DJ, Yang TP, Nicholls RD.
    Mol Hum Reprod; 1997 Apr 01; 3(4):321-32. PubMed ID: 9237260
    [Abstract] [Full Text] [Related]

  • 40. [Genomic imprinting and human hereditary pathology].
    Nemtsova MV.
    Mol Biol (Mosk); 2000 Apr 01; 34(4):646-53. PubMed ID: 11042856
    [No Abstract] [Full Text] [Related]

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