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Journal Abstract Search

229 related items for PubMed ID: 8499903

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  • 5. 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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  • 6. 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; 97(6):784-93. PubMed ID: 8641697
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  • 7. Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approach.
    Malzac P, Moncla A, Voelckel MA, Livet MO, Girardot L, Mattei MG, Mattei JF.
    Neuromuscul Disord; 1993 Jun; 3(5-6):493-6. PubMed ID: 7910502
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  • 10. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
    Procter M, Chou LS, Tang W, Jama M, Mao R.
    Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
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  • 11. Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.
    Mutirangura A, Kuwano A, Ledbetter SA, Chinault AC, Ledbetter DH.
    Hum Mol Genet; 1992 May; 1(2):139. PubMed ID: 1301155
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  • 12. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
    Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, Gillessen-Kaesbach G, Horsthemke B.
    Hum Genet; 1992 Nov; 90(3):313-5. PubMed ID: 1487250
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  • 16. 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; 3(4):321-32. PubMed ID: 9237260
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  • 20. Molecular screening for proximal 15q abnormalities in a mentally retarded population.
    Jacobsen J, King BH, Leventhal BL, Christian SL, Ledbetter DH, Cook EH.
    J Med Genet; 1998 Jul; 35(7):534-8. PubMed ID: 9678696
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