[1] Carter M,Scherer S.Autism spectrum disorder in the genetics clinic:a review[J].Clin Genet,2013,83(5):399-407. [2] Clifford SM,Hudry K,Elsabbagh M,et al.Temperament in the first 2 years of life in infants at high-risk for autism spectrum disorders[J].J Autism Dev Disord,2013,43(3):673-686. [3] Barger BD,Campbell JM,McDonough JD,Prevalence and onset of regression within autism spectrum disorders:a meta-analytic review[J].J Autism Dev Disord,2013,43(4):817-828. [4] Autism I,Developmental Disabilities Monitoring Network Surveillance Year Principal,C.Centers for Disease,et al.Prevalence of autism spectrum disorders-autism and developmental disabilities monitoring network,14 sites,United States,2008[J].MMWR Surveill Summ,2012,61(3):1-19. [5] Lundstrom,Chang SZ,Rastam M,et al.Autism spectrum disorders and autistic like traits:similar etiology in the extreme end and the normal variation[J].Arch Gen Psychiatry,2012,69(1):46-52. [6] Yang Y,Pan C.Role of metabotropic glutamate receptor 7 in autism spectrum disorders: a pilot study[J].Life Sci,2013,92(2):149-153. [7] Michaelson JJ,Shi Y,Gujral M,et al.Whole-genome sequencing in autism identifies hot spots for de novo germline mutation[J].Cell,2012,151(7):1431-1442. [8] Ferland RJ,Cherry TJ,Preware PO,et al.Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain[J].J Comp Neurol,2003,460(2):266-279. [9] Shu W,Yang H,Zhang L,et al.Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors[J].J Biol Chem,2001,276(29):27488-27497. [10] Hamdan FF,Daoud H,Rochefort D,et al.De novo mutations in FOXP1 in cases with intellectual disability,autism,and language impairment[J].Am J Hum Genet,2010,87(5):671-678. [11] Anitha A,Thanseem I,Nakamura K,et al.Protocadherin alpha (PCDHA) as a novel susceptibility gene for autism[J].J Psychiatry Neurosci,2013,38(3):192-198. [12] Krug DA,Arick J,Almond P.Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior[J].J Child Psychol Psychiatry,1980,21(3):221-229. [13] Toma C,Hervas A,Torrico B,et al.Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2[J].Psychiatr Genet,2013,23(2):82-85. [14] Teramitsu I,Kudo LC,London SE,et al.Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction[J].J Neurosci,2004,24(13):3152-3163. [15] Bacon C,Rappold GA.The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders[J].Hum Genet,2012,131(11):1687-1698. [16] Bowers JM,Konopka G.The role of the FOXP family of transcription factors in ASD[J].Dis Markers,2012,33(5):251-260. [17] Pariani MJ,Spencer A,Graham JM,et al.A 785kb deletion of 3p14.1p13,including the FOXP1 gene,associated with speech delay,contractures,hypertonia and blepharophimosis[J].Eur J Med Genet,2009,52(2-3):123-127. [18] O'Roak BJ,Deriziotis P,Lee C,et al.Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations[J].Nat Genet,2011,43(6):585-589. |