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Journal Abstract Search


229 related items for PubMed ID: 8499903

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  • 4. Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome.
    Fridman C, Koiffmann CP.
    Am J Med Genet; 2000 Sep 18; 94(3):249-53. PubMed ID: 10995513
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  • 5. A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.
    Mutirangura A, Jayakumar A, Sutcliffe JS, Nakao M, McKinney MJ, Buiting K, Horsthemke B, Beaudet AL, Chinault AC, Ledbetter DH.
    Genomics; 1993 Dec 18; 18(3):546-52. PubMed ID: 8307564
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  • 12. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
    Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, Gillessen-Kaesbach G, Horsthemke B.
    Hum Genet; 1992 Nov 18; 90(3):313-5. PubMed ID: 1487250
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  • 14. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age.
    Ginsburg C, Fokstuen S, Schinzel A.
    Am J Med Genet; 2000 Dec 18; 95(5):454-60. PubMed ID: 11146466
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  • 16. 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 18; 3(4):321-32. PubMed ID: 9237260
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  • 19. Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.
    Glenn CC, Nicholls RD, Robinson WP, Saitoh S, Niikawa N, Schinzel A, Horsthemke B, Driscoll DJ.
    Hum Mol Genet; 1993 Sep 18; 2(9):1377-82. PubMed ID: 8242060
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