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

322 related items for PubMed ID: 19793310

  • 1. Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders.
    Ozgen HM, van Daalen E, Bolton PF, Maloney VK, Huang S, Cresswell L, van den Boogaard MJ, Eleveld MJ, van 't Slot R, Hochstenbach R, Beemer FA, Barrow M, Barber JC, Poot M.
    Clin Genet; 2009 Oct; 76(4):348-56. PubMed ID: 19793310
    [Abstract] [Full Text] [Related]

  • 2. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.
    Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC, Yim SH, Yoo HK, Kim MY, Jung GY, Shin GW, Kim BN, Hwang JW, Kang JJ, Kim TM, Chung YJ.
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [Abstract] [Full Text] [Related]

  • 5. [Copy number variation analysis of a Chinese Han family with autism spectrum disorder].
    Yan G, Liang Y, Wang Y, Huang W, Zou X, Zhong N.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):654-8. PubMed ID: 21154326
    [Abstract] [Full Text] [Related]

  • 6. Autism spectrum disorders: molecular genetic advances.
    Bacchelli E, Maestrini E.
    Am J Med Genet C Semin Med Genet; 2006 Feb 15; 142C(1):13-23. PubMed ID: 16419096
    [Abstract] [Full Text] [Related]

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

  • 8. Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.
    Chung BH, Drmic I, Marshall CR, Grafodatskaya D, Carter M, Fernandez BA, Weksberg R, Roberts W, Scherer SW.
    Eur J Med Genet; 2011 Feb 15; 54(5):e516-20. PubMed ID: 21689796
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 11. Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
    Wang P, Carrion P, Qiao Y, Tyson C, Hrynchak M, Calli K, Lopez-Rangel E, Andrieux J, Delobel B, Duban-Bedu B, Thuresson AC, Annerén G, Liu X, Rajcan-Separovic E, Suzanne Lewis ME.
    Eur J Med Genet; 2013 Aug 15; 56(8):420-5. PubMed ID: 23727450
    [Abstract] [Full Text] [Related]

  • 12. Copy number variation findings among 50 children and adolescents with autism spectrum disorder.
    Sorte HS, Gjevik E, Sponheim E, Eiklid KL, Rødningen OK.
    Psychiatr Genet; 2013 Apr 15; 23(2):61-9. PubMed ID: 23277134
    [Abstract] [Full Text] [Related]

  • 13. Analysis of MECP2 gene copy number in boys with autism.
    Xi CY, Lu Y, Tan YH, Hua TY, Zhao YJ, Liu XM, Gao H.
    J Child Neurol; 2011 May 15; 26(5):570-3. PubMed ID: 21531908
    [Abstract] [Full Text] [Related]

  • 14. Etiologic yield of autistic spectrum disorders: a prospective study.
    Battaglia A, Carey JC.
    Am J Med Genet C Semin Med Genet; 2006 Feb 15; 142C(1):3-7. PubMed ID: 16419094
    [Abstract] [Full Text] [Related]

  • 15. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
    Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R.
    Neurosci Lett; 2008 Aug 15; 441(1):56-60. PubMed ID: 18597938
    [Abstract] [Full Text] [Related]

  • 16. [Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].
    He WZ, Liu WQ, Zhong XQ, Chen XL, Li SY, Zhang HM, Li Q, Cui QL, Sun XF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Jun 15; 29(3):266-9. PubMed ID: 22678785
    [Abstract] [Full Text] [Related]

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

  • 18. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
    Wang L, Fidler C, Nadig N, Giagounidis A, Della Porta MG, Malcovati L, Killick S, Gattermann N, Aul C, Boultwood J, Wainscoat JS.
    Haematologica; 2008 Jul 15; 93(7):994-1000. PubMed ID: 18508791
    [Abstract] [Full Text] [Related]

  • 19. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
    Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K.
    Genet Couns; 2004 Jul 15; 15(3):293-301. PubMed ID: 15517821
    [Abstract] [Full Text] [Related]

  • 20. Modeling clinical outcome of children with autistic spectrum disorders.
    Coplan J, Jawad AF.
    Pediatrics; 2005 Jul 15; 116(1):117-22. PubMed ID: 15995041
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 17.