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Journal Abstract Search

192 related items for PubMed ID: 7490922

  • 1.
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  • 3. Diagnostic testing: a cost analysis for Prader-Willi and Angelman syndromes.
    Monaghan KG, Van Dyke DL, Feldman G, Wiktor A, Weiss L.
    Am J Hum Genet; 1997 Jan; 60(1):244-7. PubMed ID: 8981972
    [No Abstract] [Full Text] [Related]

  • 4. [The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome].
    Iourov IY, Vorsanova SG, Kurinnaaya OS, Kolotii AD, Demidova IA, Kravets VS, Yurov YB.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2014 Jan; 114(1):49-53. PubMed ID: 24637817
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  • 5. Atypical molecular findings identify limits of technical screening tests for Prader-Willi and Angelman syndrome diagnoses.
    Malzac P, Moncla A, Pedeillier K, Vo Van C, Girardot L, Voelckel MA.
    Am J Med Genet; 1998 Jul 07; 78(3):242-4. PubMed ID: 9677058
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  • 6. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
    Santa María L, Curotto B, Cortés F, Rojas C, Alliende MA.
    Rev Med Chil; 2001 Apr 07; 129(4):367-74. PubMed ID: 11413988
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  • 7. Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities.
    Khan NL, Wood NW.
    Curr Opin Neurol; 1999 Apr 07; 12(2):149-54. PubMed ID: 10226746
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  • 9. PCR-based strategies for the diagnosis of Prader-Willi/Angelman syndromes.
    Velinov M, Jenkins EC.
    Methods Mol Biol; 2003 Apr 07; 217():209-16. PubMed ID: 12491935
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  • 10. A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.
    Chotai KA, Payne SJ.
    J Med Genet; 1998 Jun 07; 35(6):472-5. PubMed ID: 9643288
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  • 11. Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.
    Smith A, Prasad M, Deng ZM, Robson L, Woodage T, Trent RJ.
    Arch Dis Child; 1995 May 07; 72(5):397-402. PubMed ID: 7618904
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  • 13. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
    Cockwell AE, Dávalos IP, Rivera HR, Crolla JA.
    Am J Med Genet; 2001 Nov 01; 103(4):289-94. PubMed ID: 11746008
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  • 14. A new genetic test for Prader-Willi and Angelman syndromes.
    Lovell-Smith CJ, Watt AJ, Gardner RJ.
    N Z Med J; 1995 May 10; 108(999):179. PubMed ID: 7753521
    [No Abstract] [Full Text] [Related]

  • 15. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.
    Raca G, Buiting K, Das S.
    Genet Test; 2004 May 10; 8(4):387-94. PubMed ID: 15684868
    [Abstract] [Full Text] [Related]

  • 16. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
    Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S.
    Am J Hum Genet; 1994 May 10; 54(5):748-56. PubMed ID: 8178816
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  • 17. High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome.
    Butler MG.
    Am J Med Genet; 1995 May 08; 56(4):420-2. PubMed ID: 7604853
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  • 18. Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes.
    Ramsden SC, Clayton-Smith J, Birch R, Buiting K.
    BMC Med Genet; 2010 May 11; 11():70. PubMed ID: 20459762
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  • 19. Prenatal diagnosis of Prader-Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13.
    Chang CW, Hsu HK, Kao CC, Huang JY, Kuo PL.
    Int J Gynaecol Obstet; 2014 Apr 11; 125(1):18-21. PubMed ID: 24434231
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