These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


94 related items for PubMed ID: 3688026

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
    Cassidy SB, Thuline HC, Holm VA.
    Am J Med Genet; 1984 Feb; 17(2):485-95. PubMed ID: 6336316
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.
    Toth-Fejel S, Magenis RE, Leff S, Brown MG, Comegys B, Lawce H, Berry T, Kesner D, Webb MJ, Olson S.
    Am J Med Genet; 1995 Feb 13; 55(4):444-52. PubMed ID: 7762584
    [Abstract] [Full Text] [Related]

  • 9. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
    Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA.
    Am J Med Genet; 1994 Aug 01; 52(1):85-91. PubMed ID: 7977469
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
    Wiriyaukaradecha S, Patmasiriwat P, Wasant P, Tantiniti P.
    Southeast Asian J Trop Med Public Health; 2003 Dec 01; 34(4):881-6. PubMed ID: 15115105
    [Abstract] [Full Text] [Related]

  • 13. Water intake and risk of hyponatraemia in Prader-Willi syndrome.
    Akefeldt A.
    J Intellect Disabil Res; 2009 Jun 01; 53(6):521-8. PubMed ID: 19302470
    [Abstract] [Full Text] [Related]

  • 14. Non-reciprocal translocation (5;15), isodicentric (15) and Prader-Willi syndrome.
    Murdock RL, Wurster-Hill DH.
    Am J Med Genet; 1986 Sep 01; 25(1):61-9. PubMed ID: 3799724
    [Abstract] [Full Text] [Related]

  • 15. Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome.
    Rivera H, Zuffardi O, Gargantini L.
    Am J Med Genet; 1990 Nov 01; 37(3):311-7. PubMed ID: 2260556
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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 01; 28(4):829-38. PubMed ID: 3688021
    [Abstract] [Full Text] [Related]

  • 19. Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.
    Mitchell J, Schinzel A, Langlois S, Gillessen-Kaesbach G, Schuffenhauer S, Michaelis R, Abeliovich D, Lerer I, Christian S, Guitart M, McFadden DE, Robinson WP.
    Am J Med Genet; 1996 Oct 16; 65(2):133-6. PubMed ID: 8911605
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 5.