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

PUBMED FOR HANDHELDS

Journal Abstract Search

343 related items for PubMed ID: 31837200

  • 21. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE, Howley S, Murphy KC.
    Dev Disabil Res Rev; 2008; 14(1):26-34. PubMed ID: 18636634
    [Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.
    Prasad S, Katina S, Hennessy RJ, Murphy KC, Bowman AW, Waddington JL.
    Am J Med Genet A; 2015 Mar; 167A(3):529-36. PubMed ID: 25691406
    [Abstract] [Full Text] [Related]

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

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology.
    Morrison S, Chawner SJRA, van Amelsvoort TAMJ, Swillen A, Vingerhoets C, Vergaelen E, Linden DEJ, Linden S, Owen MJ, van den Bree MBM.
    Transl Psychiatry; 2020 Feb 03; 10(1):53. PubMed ID: 32066691
    [Abstract] [Full Text] [Related]

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

  • 30. The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study.
    Olszewski AK, Kikinis Z, Gonzalez CS, Coman IL, Makris N, Gong X, Rathi Y, Zhu A, Antshel KM, Fremont W, Kubicki MR, Bouix S, Shenton ME, Kates WR.
    Behav Brain Funct; 2017 Feb 16; 13(1):4. PubMed ID: 28209179
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. [22q11.2DS Syndrome as a Genetic Subtype of Schizophrenia].
    Huertas-Rodríguez CK, Payán-Gómez C, Forero-Castro RM.
    Rev Colomb Psiquiatr; 2015 Feb 16; 44(1):50-60. PubMed ID: 26578219
    [Abstract] [Full Text] [Related]

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

  • 35. Does differential visual exploration contribute to visual memory impairments in 22q11.2 microdeletion syndrome?
    Bostelmann M, Glaser B, Zaharia A, Eliez S, Schneider M.
    J Intellect Disabil Res; 2017 Dec 16; 61(12):1174-1184. PubMed ID: 29154491
    [Abstract] [Full Text] [Related]

  • 36. Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome.
    Yi JJ, Tang SX, McDonald-McGinn DM, Calkins ME, Whinna DA, Souders MC, Zackai EH, Goldmuntz E, Gaynor JW, Gur RC, Emanuel BS, Gur RE.
    Am J Med Genet B Neuropsychiatr Genet; 2014 Mar 16; 165B(2):137-47. PubMed ID: 24265253
    [Abstract] [Full Text] [Related]

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

  • 38. Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.
    Van Aken K, Swillen A, Beirinckx M, Janssens L, Caeyenberghs K, Smits-Engelsman B.
    Res Dev Disabil; 2010 Mar 16; 31(3):634-41. PubMed ID: 20181458
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome.
    Cunningham AC, Hill L, Mon-Williams M, Peall KJ, Linden DEJ, Hall J, Owen MJ, van den Bree MBM.
    J Neurodev Disord; 2019 Jun 10; 11(1):8. PubMed ID: 31182009
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 18.