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Journal Abstract Search

234 related items for PubMed ID: 15930057

  • 1. Lower prepulse inhibition in children with the 22q11 deletion syndrome.
    Sobin C, Kiley-Brabeck K, Karayiorgou M.
    Am J Psychiatry; 2005 Jun; 162(6):1090-9. PubMed ID: 15930057
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  • 6. Dependency of prepulse inhibition deficits on baseline startle reactivity in a mouse model of the human 22q11.2 microdeletion syndrome.
    Scarborough J, Mueller F, Weber-Stadlbauer U, Richetto J, Meyer U.
    Genes Brain Behav; 2019 Apr; 18(4):e12523. PubMed ID: 30267483
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  • 11. Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.
    Paylor R, McIlwain KL, McAninch R, Nellis A, Yuva-Paylor LA, Baldini A, Lindsay EA.
    Hum Mol Genet; 2001 Nov 01; 10(23):2645-50. PubMed ID: 11726551
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  • 12. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec 01; 35(4):248-51. PubMed ID: 23834556
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  • 13. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
    Pinquier C, Héron D, de Carvalho W, Lazar G, Mazet P, Cohen D.
    Encephale; 2001 Dec 01; 27(1):45-50. PubMed ID: 11294038
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  • 17. [Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].
    Briegel W, Cohen M.
    Z Kinder Jugendpsychiatr Psychother; 2004 May 01; 32(2):107-15. PubMed ID: 15181786
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  • 20. Attenuated positive symptoms of psychosis in adolescents with chromosome 22q11.2 deletion syndrome.
    Stoddard J, Niendam T, Hendren R, Carter C, Simon TJ.
    Schizophr Res; 2010 May 01; 118(1-3):118-21. PubMed ID: 20056393
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