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Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.

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第一作者: Jennifer L,Roberts
第一单位: Departments of Psychiatry, Behavioral Sciences and Pediatrics, The University of Kansas, Medical Center, Kansas City, KS, USA.
作者单位: Departments of Psychiatry, Behavioral Sciences and Pediatrics, The University of Kansas, Medical Center, Kansas City, KS, USA. [1] CombiMatrix Diagnostics, Irvine, CA, USA. [2] Department of Neurology, The University of Kansas Medical Center, Kansas City, KS, USA; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. [3] Departments of Psychiatry, Behavioral Sciences and Pediatrics, The University of Kansas, Medical Center, Kansas City, KS, USA. Electronic address: mbutler4@kumc.edu. [4]
关键词 A2BP1ACADLACOXLADIPOQALS2 chromosome region gene 8ALS2CR8ANKRD11ANOVAASDAutism spectrum disorders (ASD)BACBCL2-like 11 geneBCL2L11CACNA1CCHRNA7CNVCOBLCTChromosomal microarray analysisCopy number variant (CNV)DLG1DLG4DNADevelopmental delayEEF1B2EEGF-box only 45 geneFAM117BFAT tumor suppressor 1 geneFAT1FBXO45FISHFXR2FZD5GALR1GATA zinc finger domain-containing protein 2B geneGATAD2BGDNF-inducible zinc finger protein 1 geneGZF1HAX1HCLS1-associated protein X1 geneHDACIDH1IL1RAPL1ITPR1KLF7KNG1LINSLMNALearning disabilityMAP2MBPMRPL19MYL1NADH-ubiquinone oxidoreductase Fe-S protein 1 geneNDUFS1NLGN2NPHP1NRXN1PAK2PARK2PMP22POLGPRPF8PTENPTH2RRPESACSSDSH2B adaptor protein 1 geneSH2B1SH3 and multiple ankyrin repeat domains 3 geneSHANK3SHOXSMARCA4STAG2SUMF1SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member geneTRAPPC2UCSCUSP6University of California, Santa CruzX-linked inhibitor of apoptosis geneXIAPYWHAEZNF407aCGHacyl-coA dehydrogenase, long chain geneacyl-coA oxidase-like geneadipocyte-, C1q-, and collagen domain containing geneanalysis of varianceankyrin repeat domain-containing protein 11 genearray comparative genomic hybridizationataxin 2-binding protein 1 geneautism spectrum disorderbacterial artificial chromosomecalcium channel, voltage dependent, L-type, alpha 1C subunit genecholinergic receptor, neuronal nicotinic, alpha polypeptide 7 genecomputed tomographycopy number variantcordon-bleu genedeoxyribonucleic aciddiscs, large homolog 1 genediscs, large homolog 4 geneelectroencephalogrameukaryotic translation elongation factor 1, beta-2 genefamily with sequence similarity 117, member B genefluorescence in situ hybridizationfragile X mental retardation, autosomal homolog 2 genefrizzled 5 genegalanin receptor 1 genehistone deacetylase geneinositol 1,4,5-triphosphate receptor, type 1 geneinterleukin 1 receptor accessory protein-like 1 geneisocitrate dehydrogenase 1 genekininogen 1 genekruppel-like factor 7 genelamin A genelines homolog genemicrotubule-associated protein 2 genemitochondrial ribosomal protein L19 genemyelin basic protein genemyosin, light peptide 1 genenephrocystin 1 geneneurexin 1 geneneuroligin 2 geneparathyroid hormone receptor 2 geneparkin geneperipheral myelin protein 22 genephosphatase and tensin homolog genepolymerase gamma geneprecursor mRNA-processing factor 8 geneprotein-activated kinase 2 generibulose 5-phosphate 3-epimerase genesacsin geneshort stature homeobox genestandard deviationstromal antigen 2 genesulfatase-modifying factor 1 genetracking protein particle complex, subunit 2 genetyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon isoform geneubiquitin-specific protease 6 genezinc finger protein 407 gene
DOI 10.1016/j.gene.2013.10.020
PMID 24188901
发布时间 2024-03-23
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