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Journal Abstract Search

215 related items for PubMed ID: 8388764

  • 1. 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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  • 2. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
    Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC.
    Hum Mol Genet; 1992 Sep; 1(6):417-25. PubMed ID: 1363801
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  • 3. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.
    Knoll JH, Cheng SD, Lalande M.
    Nat Genet; 1994 Jan; 6(1):41-6. PubMed ID: 8136833
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  • 5. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
    Christian SL, Robinson WP, Huang B, Mutirangura A, Line MR, Nakao M, Surti U, Chakravarti A, Ledbetter DH.
    Am J Hum Genet; 1995 Jul; 57(1):40-8. PubMed ID: 7611294
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  • 6. 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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  • 7. 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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  • 8. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
    Erdel M, Schuffenhauer S, Buchholz B, Barth-Witte U, Köchl S, Utermann B, Duba HC, Utermann G.
    Hum Genet; 1996 Jun 01; 97(6):784-93. PubMed ID: 8641697
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  • 9. FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.
    Teshima I, Chadwick D, Chitayat D, Kobayashi J, Ray P, Shuman C, Siegel-Bartelt J, Strasberg P, Weksberg R.
    Am J Med Genet; 1996 Mar 29; 62(3):217-23. PubMed ID: 8882776
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  • 12. Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13.
    Dittrich B, Knoblauch H, Buiting K, Horsthemke B.
    Genomics; 1993 Apr 29; 16(1):269-71. PubMed ID: 8486372
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  • 13. Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.
    Mutirangura A, Greenberg F, Butler MG, Malcolm S, Nicholls RD, Chakravarti A, Ledbetter DH.
    Hum Mol Genet; 1993 Feb 29; 2(2):143-51. PubMed ID: 8499903
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  • 14. Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.
    Christian SL, Bhatt NK, Martin SA, Sutcliffe JS, Kubota T, Huang B, Mutirangura A, Chinault AC, Beaudet AL, Ledbetter DH.
    Genome Res; 1998 Feb 29; 8(2):146-57. PubMed ID: 9477342
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  • 15. 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 Feb 29; 81(3-4):247-53. PubMed ID: 9730612
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  • 16. Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.
    Nicholls RD, Gottlieb W, Russell LB, Davda M, Horsthemke B, Rinchik EM.
    Proc Natl Acad Sci U S A; 1993 Mar 01; 90(5):2050-4. PubMed ID: 8095339
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  • 18. Molecular study of chromosome 15 in 22 patients with Angelman syndrome.
    Beuten J, Mangelschots K, Buntinx I, Coucke P, Brouwer OF, Hennekam RC, Van Broeckhoven C, Willems PJ.
    Hum Genet; 1993 Jan 01; 90(5):489-95. PubMed ID: 8094063
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