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Journal Abstract Search

388 related items for PubMed ID: 7987392

  • 1. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region.
    Sutcliffe JS, Nakao M, Christian S, Orstavik KH, Tommerup N, Ledbetter DH, Beaudet AL.
    Nat Genet; 1994 Sep; 8(1):52-8. PubMed ID: 7987392
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  • 2. 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; 12(4):452-4. PubMed ID: 8630505
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  • 3. Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.
    Ozçelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, Francke U.
    Nat Genet; 1992 Dec; 2(4):265-9. PubMed ID: 1303277
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  • 4. The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
    Bressler J, Tsai TF, Wu MY, Tsai SF, Ramirez MA, Armstrong D, Beaudet AL.
    Nat Genet; 2001 Jul; 28(3):232-40. PubMed ID: 11431693
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  • 6. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
    Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B.
    Nat Genet; 1995 Apr; 9(4):395-400. PubMed ID: 7795645
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  • 7. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
    Zeschnigk M, Schmitz B, Dittrich B, Buiting K, Horsthemke B, Doerfler W.
    Hum Mol Genet; 1997 Mar; 6(3):387-95. PubMed ID: 9147641
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  • 9. Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region.
    Leff SE, Brannan CI, Reed ML, Ozçelik T, Francke U, Copeland NG, Jenkins NA.
    Nat Genet; 1992 Dec; 2(4):259-64. PubMed ID: 1303276
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  • 10. Mouse imprinting defect mutations that model Angelman syndrome.
    Wu MY, Chen KS, Bressler J, Hou A, Tsai TF, Beaudet AL.
    Genesis; 2006 Jan; 44(1):12-22. PubMed ID: 16397868
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  • 13. A mouse model for Prader-Willi syndrome imprinting-centre mutations.
    Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI.
    Nat Genet; 1998 May; 19(1):25-31. PubMed ID: 9590284
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  • 14. In and around SNRPN.
    Lalande M.
    Nat Genet; 1994 Sep; 8(1):5-7. PubMed ID: 7987391
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  • 17. Methylation analysis at three different loci within the imprinted region of chromosome 15q11-13.
    Buchholz T, Jackson J, Smith A.
    Am J Med Genet; 1997 Oct 03; 72(1):117-9. PubMed ID: 9295088
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  • 20. Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR method.
    Kosaki K, McGinniss MJ, Veraksa AN, McGinnis WJ, Jones KL.
    Am J Med Genet; 1997 Dec 19; 73(3):308-13. PubMed ID: 9415690
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