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Journal Abstract Search

302 related items for PubMed ID: 8136833

  • 1. 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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  • 2. 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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  • 3. Parental imprinting and Angelman syndrome.
    Lalande M, Minassian BA, DeLorey TM, Olsen RW.
    Adv Neurol; 1999 Jan 01; 79():421-9. PubMed ID: 10514831
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  • 4. The imprinting box of the Prader-Willi/Angelman syndrome domain.
    Shemer R, Hershko AY, Perk J, Mostoslavsky R, Tsuberi B, Cedar H, Buiting K, Razin A.
    Nat Genet; 2000 Dec 01; 26(4):440-3. PubMed ID: 11101841
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  • 5. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Schulze A, Hansen C, Skakkebaek NE, Brøndum-Nielsen K, Ledbeter DH, Tommerup N.
    Nat Genet; 1996 Apr 01; 12(4):452-4. PubMed ID: 8630505
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  • 6. Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution.
    LaSalle JM, Lalande M.
    Nat Genet; 1995 Apr 01; 9(4):386-94. PubMed ID: 7795644
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  • 7. Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).
    Park JP, Moeschler JB, Hani VH, Hawk AB, Belloni DR, Noll WW, Mohandas TK.
    Am J Med Genet; 1998 Jun 30; 78(2):134-9. PubMed ID: 9674903
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  • 8. 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 30; 2(2):183-9. PubMed ID: 8388764
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  • 9. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.
    Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roëckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F.
    Nat Genet; 1997 Nov 30; 17(3):357-61. PubMed ID: 9354807
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  • 12. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G, Novotna D, Simandlova M, Havlovicova M, Zumrová A, Kocarek E, Sedlacek Z.
    Neuro Endocrinol Lett; 2006 Oct 30; 27(5):579-85. PubMed ID: 17159828
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  • 13. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD.
    Am J Med Genet; 1993 Oct 01; 47(5):683-6. PubMed ID: 8266996
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  • 15. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
    Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD.
    Am J Med Genet; 1997 Jan 20; 68(2):195-206. PubMed ID: 9028458
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  • 19. Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.
    Gurrieri F, Accadia M.
    Endocr Dev; 2009 Jan 20; 14():20-8. PubMed ID: 19293572
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