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Journal Abstract Search

312 related items for PubMed ID: 20613623

  • 1. Cognitive and behavioral characterization of 16p11.2 deletion syndrome.
    Hanson E, Nasir RH, Fong A, Lian A, Hundley R, Shen Y, Wu BL, Holm IA, Miller DT, 16p11.2 Study Group Clinicians.
    J Dev Behav Pediatr; 2010 Oct; 31(8):649-57. PubMed ID: 20613623
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW.
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
    [Abstract] [Full Text] [Related]

  • 3. Association between microdeletion and microduplication at 16p11.2 and autism.
    Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, Tanzi RE, Stefansson K, Santangelo SL, Gusella JF, Sklar P, Wu BL, Daly MJ, Autism Consortium.
    N Engl J Med; 2008 Feb 14; 358(7):667-75. PubMed ID: 18184952
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  • 4. A case of 8q22.1 microdeletion without the Nablus mask-like facial syndrome phenotype.
    Jain S, Yang P, Farrell SA.
    Eur J Med Genet; 2010 Feb 14; 53(2):108-10. PubMed ID: 20074678
    [Abstract] [Full Text] [Related]

  • 5. Structure of the autism symptom phenotype: A proposed multidimensional model.
    Georgiades S, Szatmari P, Zwaigenbaum L, Duku E, Bryson S, Roberts W, Goldberg J, Mahoney W.
    J Am Acad Child Adolesc Psychiatry; 2007 Feb 14; 46(2):188-96. PubMed ID: 17242622
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  • 6. Developmental profiles in preschool children with autism spectrum disorders referred for intervention.
    Fernell E, Hedvall A, Norrelgen F, Eriksson M, Höglund-Carlsson L, Barnevik-Olsson M, Svensson L, Holm A, Westerlund J, Gillberg C.
    Res Dev Disabil; 2010 Feb 14; 31(3):790-9. PubMed ID: 20207104
    [Abstract] [Full Text] [Related]

  • 7. A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.
    Shimojima K, Inoue T, Fujii Y, Ohno K, Yamamoto T.
    Eur J Med Genet; 2009 Feb 14; 52(6):433-5. PubMed ID: 19770079
    [Abstract] [Full Text] [Related]

  • 8. Recurrent 16p11.2 microdeletions in autism.
    Kumar RA, KaraMohamed S, Sudi J, Conrad DF, Brune C, Badner JA, Gilliam TC, Nowak NJ, Cook EH, Dobyns WB, Christian SL.
    Hum Mol Genet; 2008 Feb 15; 17(4):628-38. PubMed ID: 18156158
    [Abstract] [Full Text] [Related]

  • 9. Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.
    Peters SU, Horowitz L, Barbieri-Welge R, Taylor JL, Hundley RJ.
    J Child Psychol Psychiatry; 2012 Feb 15; 53(2):152-9. PubMed ID: 21831244
    [Abstract] [Full Text] [Related]

  • 10. Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a de novo deletion on chromosome 16q23.2.
    Van der Aa N, Vandeweyer G, Reyniers E, Kenis S, Dom L, Mortier G, Rooms L, Kooy RF.
    Autism Res; 2012 Aug 15; 5(4):277-81. PubMed ID: 22689534
    [Abstract] [Full Text] [Related]

  • 11. The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals.
    Niklasson L, Gillberg C.
    Res Dev Disabil; 2010 Aug 15; 31(1):185-94. PubMed ID: 19815377
    [Abstract] [Full Text] [Related]

  • 12. [Autism, genetics and synaptic function alterations].
    Perche O, Laumonnier F, Baala L, Ardourel MY, Menuet A, Robin V, Mortaud S, Montécot-Dubourg C, Richard O, Pichon J, Briault S.
    Pathol Biol (Paris); 2010 Oct 15; 58(5):381-6. PubMed ID: 20181440
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  • 16. Siblings of individuals with autism spectrum disorders across the life course.
    Orsmond GI, Seltzer MM.
    Ment Retard Dev Disabil Res Rev; 2007 Oct 15; 13(4):313-20. PubMed ID: 17979200
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  • 17. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
    Galasso C, Lo-Castro A, Lalli C, Nardone AM, Gullotta F, Curatolo P.
    J Child Neurol; 2008 Jul 15; 23(7):802-6. PubMed ID: 18658079
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  • 19. Aberrant behaviors of young boys with fragile X syndrome.
    Lachiewicz AM, Spiridigliozzi GA, Gullion CM, Ransford SN, Rao K.
    Am J Ment Retard; 1994 Mar 15; 98(5):567-79. PubMed ID: 8192902
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  • 20. Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation.
    Yang Y, Wang C, Wang F, Zhu L, Liu H, He X.
    Gene; 2012 Jul 10; 502(2):154-8. PubMed ID: 22555022
    [Abstract] [Full Text] [Related]

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