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Journal Abstract Search

498 related items for PubMed ID: 1363801

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  • 5. FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions.
    Knoll JH, Sinnett D, Wagstaff J, Glatt K, Wilcox AS, Whiting PM, Wingrove P, Sikela JM, Lalande M.
    Hum Mol Genet; 1993 Feb; 2(2):183-9. PubMed ID: 8388764
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  • 8. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
    Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH.
    Hum Mol Genet; 1999 Jun; 8(6):1025-37. PubMed ID: 10332034
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  • 9. Physical mapping studies at D15S10: implications for candidate gene identification in the Angelman syndrome/Prader-Willi syndrome chromosome region of 15q11-q13.
    Woodage T, Lindeman R, Deng ZM, Fimmel A, Smith A, Trent RJ.
    Genomics; 1994 Jan 01; 19(1):170-2. PubMed ID: 8188222
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  • 16. FISH analysis in Prader-Willi and Angelman syndrome patients.
    Bettio D, Rizzi N, Giardino D, Grugni G, Briscioli V, Selicorni A, Carnevale F, Larizza L.
    Am J Med Genet; 1995 Mar 27; 56(2):224-8. PubMed ID: 7625450
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  • 18. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
    Wevrick R, Kerns JA, Francke U.
    Hum Mol Genet; 1994 Oct 27; 3(10):1877-82. PubMed ID: 7849716
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  • 19. DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63).
    van den Ouweland AM, van der Est MN, Wesby-van Swaay E, Tijmensen TS, Los FJ, Van Hemel JO, Hennekam RC, Meijers-Heijboer HJ, Niermeijer MF, Halley DJ.
    Hum Genet; 1995 May 27; 95(5):562-7. PubMed ID: 7759079
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  • 20. Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
    Buiting K, Gross S, Ji Y, Senger G, Nicholls RD, Horsthemke B.
    Cytogenet Cell Genet; 1998 May 27; 81(3-4):247-53. PubMed ID: 9730612
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