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


127 related items for PubMed ID: 20981774

  • 21. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE, Dennis NR, Browne CE, Willatt L, Woods G, Cross I, Jacobs PA, Thomas S.
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [Abstract] [Full Text] [Related]

  • 22. Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndrome.
    Battaglia A, Bernardini L, Torrente I, Novelli A, Scarselli G.
    Am J Med Genet A; 2016 Oct; 170(10):2531-9. PubMed ID: 27513709
    [Abstract] [Full Text] [Related]

  • 23. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
    [Abstract] [Full Text] [Related]

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

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Rearrangements of chromosome 15 in epilepsy.
    Torrisi L, Sangiorgi E, Russo L, Gurrieri F.
    Am J Med Genet; 2001 Sep; 106(2):125-8. PubMed ID: 11579432
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.
    Bolton PF, Dennis NR, Browne CE, Thomas NS, Veltman MW, Thompson RJ, Jacobs P.
    Am J Med Genet; 2001 Dec 08; 105(8):675-85. PubMed ID: 11803514
    [Abstract] [Full Text] [Related]

  • 31. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age.
    Ginsburg C, Fokstuen S, Schinzel A.
    Am J Med Genet; 2000 Dec 18; 95(5):454-60. PubMed ID: 11146466
    [Abstract] [Full Text] [Related]

  • 32. [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]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Neurological features and long-term follow-up in 15q11.2-13.1 duplication.
    Coppola A, Ruosi P, Santulli L, Striano S, Zara F, Striano P, Sisodiya SM.
    Eur J Med Genet; 2013 Nov 08; 56(11):614-8. PubMed ID: 24075935
    [Abstract] [Full Text] [Related]

  • 40. Three probands with autistic disorder and isodicentric chromosome 15.
    Wolpert CM, Menold MM, Bass MP, Qumsiyeh MB, Donnelly SL, Ravan SA, Vance JM, Gilbert JR, Abramson RK, Wright HH, Cuccaro ML, Pericak-Vance MA.
    Am J Med Genet; 2000 Jun 12; 96(3):365-72. PubMed ID: 10898916
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 7.