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Journal Abstract Search

1446 related items for PubMed ID: 23711909

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  • 7. Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation.
    Hu T, Zhang Z, Wang J, Li Q, Zhu H, Lai Y, Wang H, Liu S.
    Biomed Res Int; 2019; 2019():9352581. PubMed ID: 31781653
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  • 9. Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.
    Nicholl J, Waters W, Mulley JC, Suwalski S, Brown S, Hull Y, Barnett C, Haan E, Thompson EM, Liebelt J, Mcgregor L, Harbord MG, Entwistle J, Munt C, White D, Chitti A, Baulderstone D, Ketteridge D, Array Referral Consortium, Friend K, Bain SM, Yu S.
    Pathology; 2014 Jan; 46(1):41-5. PubMed ID: 24300712
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  • 10. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
    Wayhelova M, Smetana J, Vallova V, Hladilkova E, Filkova H, Hanakova M, Vilemova M, Nikolova P, Gromesova B, Gaillyova R, Kuglik P.
    BMC Med Genomics; 2019 Jul 23; 12(1):111. PubMed ID: 31337399
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  • 12. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
    Cappuccio G, Vitiello F, Casertano A, Fontana P, Genesio R, Bruzzese D, Ginocchio VM, Mormile A, Nitsch L, Andria G, Melis D.
    Ital J Pediatr; 2016 Apr 12; 42():39. PubMed ID: 27072107
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  • 16. Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
    Ho KS, Twede H, Vanzo R, Harward E, Hensel CH, Martin MM, Page S, Peiffer A, Mowery-Rushton P, Serrano M, Wassman ER.
    Biomed Res Int; 2016 Apr 12; 2016():3284534. PubMed ID: 27975050
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  • 19. 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 12; 56(8):420-5. PubMed ID: 23727450
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  • 20. Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
    Ho KS, Wassman ER, Baxter AL, Hensel CH, Martin MM, Prasad A, Twede H, Vanzo RJ, Butler MG.
    Int J Mol Sci; 2016 Dec 09; 17(12):. PubMed ID: 27941670
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