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Journal Abstract Search

432 related items for PubMed ID: 9477342

  • 1.
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  • 2. 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(3):546-52. PubMed ID: 8307564
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  • 3. 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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  • 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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  • 7. A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb.
    Bouffard GG, Idol JR, Braden VV, Iyer LM, Cunningham AF, Weintraub LA, Touchman JW, Mohr-Tidwell RM, Peluso DC, Fulton RS, Ueltzen MS, Weissenbach J, Magness CL, Green ED.
    Genome Res; 1997 Jul; 7(7):673-92. PubMed ID: 9253597
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  • 8. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
    Lee S, Wevrick R.
    Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201
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  • 10. Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes.
    Makoff AJ, Flomen RH.
    Genome Biol; 2007 Mar; 8(6):R114. PubMed ID: 17573966
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  • 11. A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region.
    Mitsuda N, Nakura J, Ye L, Zhao Y, Fujioka Y, Takahashi-Fujii A, Ishino Y, Kato I, Hashimoto K, Ogihara T, Miki T.
    Genomics; 1997 Apr 01; 41(1):49-55. PubMed ID: 9126481
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  • 12. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC, Driscoll DJ, Yang TP, Nicholls RD.
    Mol Hum Reprod; 1997 Apr 01; 3(4):321-32. PubMed ID: 9237260
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  • 15. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
    [Abstract] [Full Text] [Related]

  • 16. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
    Saitoh S, Buiting K, Rogan PK, Buxton JL, Driscoll DJ, Arnemann J, König R, Malcolm S, Horsthemke B, Nicholls RD.
    Proc Natl Acad Sci U S A; 1996 Jul 23; 93(15):7811-5. PubMed ID: 8755558
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  • 17. 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 23; 16(1):269-71. PubMed ID: 8486372
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  • 19. A sequence-ready map for human chromosome 12q15-21.
    Lee SG, Cho KA, Choi YH, Montgomery K, Lee E, Miller A, Kucherlapati R, Song K.
    DNA Seq; 2000 Apr 23; 11(3-4):353-61. PubMed ID: 11092752
    [Abstract] [Full Text] [Related]

  • 20. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L, Chamberlain SJ.
    Pediatr Clin North Am; 2015 Jun 23; 62(3):587-606. PubMed ID: 26022164
    [Abstract] [Full Text] [Related]

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