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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]