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227 related items for PubMed ID: 2786338

  • 1. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.
    Williams CA, Gray BA, Hendrickson JE, Stone JW, Cantú ES.
    Am J Med Genet; 1989 Mar; 32(3):339-45. PubMed ID: 2786338
    [Abstract] [Full Text] [Related]

  • 2. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
    Magenis RE, Toth-Fejel S, Allen LJ, Black M, Brown MG, Budden S, Cohen R, Friedman JM, Kalousek D, Zonana J.
    Am J Med Genet; 1990 Mar; 35(3):333-49. PubMed ID: 2309780
    [Abstract] [Full Text] [Related]

  • 3. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.
    Kaplan LC, Wharton R, Elias E, Mandell F, Donlon T, Latt SA.
    Am J Med Genet; 1987 Sep; 28(1):45-53. PubMed ID: 3674117
    [Abstract] [Full Text] [Related]

  • 4. Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry.
    Cooke A, Tolmie JL, Glencross FJ, Boyd E, Clarke MM, Day R, Stephenson JB, Connor JM.
    Am J Med Genet; 1989 Apr; 32(4):545-9. PubMed ID: 2774001
    [Abstract] [Full Text] [Related]

  • 5. Is Angelman syndrome an alternate result of del(15)(q11q13)?
    Magenis RE, Brown MG, Lacy DA, Budden S, LaFranchi S.
    Am J Med Genet; 1987 Dec; 28(4):829-38. PubMed ID: 3688021
    [Abstract] [Full Text] [Related]

  • 6. Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.
    Williams CA, Zori RT, Stone JW, Gray BA, Cantu ES, Ostrer H.
    Am J Med Genet; 1990 Mar; 35(3):350-3. PubMed ID: 2309781
    [Abstract] [Full Text] [Related]

  • 7. [Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome].
    Mujica P, Leheup B, Gilgenkrantz S, Karp JC, Pierson M.
    J Genet Hum; 1989 Jan; 37(1):77-86. PubMed ID: 2715785
    [Abstract] [Full Text] [Related]

  • 8. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
    Knoll JH, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA.
    Am J Med Genet; 1989 Feb; 32(2):285-90. PubMed ID: 2564739
    [Abstract] [Full Text] [Related]

  • 9. Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).
    Scheuerle A, Zenger-Hain JL, Van Dyke DL, Ledbetter DH, Greenberg F, Shaffer LG.
    Am J Med Genet; 1995 May 08; 56(4):403-8. PubMed ID: 7604850
    [Abstract] [Full Text] [Related]

  • 10. Interstitial 15q deletion without a classic Prader-Willi phenotype.
    Galán F, Aguilar MS, González J, Clemente F, Sánchez R, Tapia M, Moya M.
    Am J Med Genet; 1991 Mar 15; 38(4):532-4. PubMed ID: 2063892
    [Abstract] [Full Text] [Related]

  • 11. [The Angelman syndrome. Does the phenotype depend on maternal inheritance?].
    Lund AM.
    Ugeskr Laeger; 1991 Jul 08; 153(28):1993-8. PubMed ID: 1862581
    [Abstract] [Full Text] [Related]

  • 12. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
    Luke S, Verma RS, Giridharan R, Conte RA, Macera MJ.
    Am J Med Genet; 1994 Jul 01; 51(3):232-3. PubMed ID: 7521122
    [Abstract] [Full Text] [Related]

  • 13. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):813-20. PubMed ID: 3688019
    [Abstract] [Full Text] [Related]

  • 14. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
    Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):791-802. PubMed ID: 3688017
    [Abstract] [Full Text] [Related]

  • 15. Chromosome 10qter deletion syndrome: a review and report of three new cases.
    Wulfsberg EA, Weaver RP, Cunniff CM, Jones MC, Jones KL.
    Am J Med Genet; 1989 Mar 01; 32(3):364-7. PubMed ID: 2658586
    [Abstract] [Full Text] [Related]

  • 16. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Kousseff BG, Diamond T, Essig Y, Miller K, Tedesco T.
    Am J Med Genet; 1987 Dec 01; 28(4):803-11. PubMed ID: 3688018
    [Abstract] [Full Text] [Related]

  • 17. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
    Sahoo T, Bacino CA, German JR, Shaw CA, Bird LM, Kimonis V, Anselm I, Waisbren S, Beaudet AL, Peters SU.
    Eur J Hum Genet; 2007 Sep 01; 15(9):943-9. PubMed ID: 17522620
    [Abstract] [Full Text] [Related]

  • 18. Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region.
    Michaelis RC, Skinner SA, Lethco BA, Simensen RJ, Donlon TA, Tarleton J, Phelan MC.
    Am J Med Genet; 1995 Jan 02; 55(1):120-6. PubMed ID: 7702085
    [Abstract] [Full Text] [Related]

  • 19. [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 02; 129(4):367-74. PubMed ID: 11413988
    [Abstract] [Full Text] [Related]

  • 20. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB, Zackai E, Cheng SD, Knoll JH.
    Am J Med Genet; 1995 May 22; 57(1):61-5. PubMed ID: 7645601
    [Abstract] [Full Text] [Related]

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