[Anonymous (1992). The ICD-10 classification of mental and behavioural disorders; clinical description and diagnostic guidelines. World Health Organization. Geneva, WHO.]Search in Google Scholar
[Anonymous (1994). Diagnosis and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV). American Psychiatric Association. Washington DC: American Psychiatric Publishing.]Search in Google Scholar
[Bailley, A., Phillips, W., Rutter, M. (1996). Autism: Towards an integration of clinical, genetic, neuropsychological and neurobiological perspectives. J. Child Psychol. Psychiatry, 37, 89–126.10.1111/j.1469-7610.1996.tb01381.x8655659]Search in Google Scholar
[Baron-Cohen, S., Allen, J., Gillberg, C. (1992). Can autism be detected at 18 month? The needle, the haystack, and the CHAT. Br. J. Psychiatry, 161, 839–843.10.1192/bjp.161.6.8391483172]Search in Google Scholar
[Baron-Cohen, S., Hoekstra, A. R., Knickmeyer, R., Wheelwright, S. (2006). The Autism Quotient (AQ) — adolescent version. J. Autism Devel. Disord., 36, 343–350.10.1007/s10803-006-0073-616552625]Search in Google Scholar
[Cho, S. C., Yoo, H. J., Park, M., Cho, I. H., Kim, B. N., Kim, J. W., Shin, M. S., Park, T. W., Son, J. W., Chung, U. S., Kim, H. W., Yang, Y. H., Kang, J. O., Yang, S. Y., Kim, S. A. (2011). Genome–wide association scan of Korean autism spectrum disorders with language delay: A preliminary study. Psychiatry Investig., 8, 61–66.10.4306/pi.2011.8.1.61307918821519539]Search in Google Scholar
[Gillberg, C. (2006). Autism spectrum disorders. In: Gillberg, C., Harrington, R., Steinhausen, H. C. (eds.). A Clinician’s Handbook of Child and Adolescent Psychiatry (pp. 447–489). UK Cambridge University Press.]Search in Google Scholar
[Johnson, C. P., Myuer, S. M. (2007). Identification and evaluation of children with autism spectrum sisorders. Pediatrics, 120, 1183–1215.10.1542/peds.2007-236117967920]Search in Google Scholar
[Johnson, H. M., Gaitanis, J., Morrow, E. M. (2011). Genetics in autism diagnosis: Adding molecular subtypes to neurobehavioral diagnoses. Medical Health R. I., 94, 124–126.]Search in Google Scholar
[Kondo, H., Shirakawa, R., Higashi, T., Kawato, M., Fukuda, M., Kita, T., Horiuchi, H. (2006). Constitutive GDP/GTP exchange and secretion-dependent GTP hydrolysis activity for Rab27 in platelets. J. Biol. Chem., 29 (281), 28657–28665.10.1074/jbc.M60322720016880209]Search in Google Scholar
[Lintas, C., Persico, A. M. (2009). Autistic phenotypes and genetic testing: State-of-the art for the clinical geneticist. J. Med. Genet., 46, 1–8.10.1136/jmg.2008.060871260348118728070]Search in Google Scholar
[Liu, X. Q., Paterson, A. D., Szatmari, P. (2008). Genome-wide linkage analyses of quantitative and categorical autism subphenotypes. J. Biol. Psychiatry, 647, 561–570.10.1016/j.biopsych.2008.05.023267097018632090]Search in Google Scholar
[Lord, C., Rutter, M., DiLavore, P. C., Risi, S. (2002). Autism Diagnostic Observation Scedule. Manual. Los Angeles: Western Psychological Services.]Search in Google Scholar
[Muhle, R., Trentacoste, S. V., Rapin, I. (2004). The genetics of autism. Pediatrics, 113 (5), 472–486.10.1542/peds.113.5.e47215121991]Search in Google Scholar
[Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A., Bender, D., Maller, J., Sklar, J., de Bakker, P. I., Daly, M. J., Sham, P. C. (2007). PLINK: A tool set for whole-genome association and population-based linkage analyses. Eur. J. Hum. Genet., 81, 559–575.10.1086/519795195083817701901]Search in Google Scholar
[Risch, N., Spiker, D., Lotspeich, L., Nourj, N., Hinds, D., Hallmayer, J., Kalaydjieva, L., McCague, P., Dimiceli, S., Pitts, T., Nguyen, L., Yang, J., Harper, C., Thorpe, D., Vermeer, S., Young, H., Hebert, J., Lin, A., Ferguson, J., Chiotti, C., Wiese-Slater, S., Rogers, T., Salmon, B., Nicholas, P., Petersen, P. B., Pingree, C., McMahon, W., Wong, D. L., Cavalli-Sforza, L. L., Kraemer, H. C., Myers, R. M. (1999). A genomic screen of autism: Evidence for a multilocus etiology. Amer. J. Hum. Genet., 65, 493–507.10.1086/302497137794810417292]Search in Google Scholar
[Sambrook, J., Fritsch, E. F., Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual. Cold Spring Harbor: Cold Spring Harbor Laboratory Press.]Search in Google Scholar
[Savitsky, K., Ziv, Y., Bar-Shira, A., Gilad, S., Tagle, D. A., Smith, S., Uziel, T., Sfez, S., Nahmias, J., Sartiel, A., Eddy, R. L., Shows, T. B., Collins, F. S., Shiloh, Y., Rotman, G. (1996). A human gene (DDX10) encoding a putative DEAD-box RNA helcase at 11q22-q23. Genomics, 15 (33), 199–206.10.1006/geno.1996.01848660968]Search in Google Scholar
[Scott, F. J., Baron-Cohen, S., Bolton, P., Brayne, C. (2002). The CAST (Childhood Asperger Syndrome Test): Preliminary development of a UK screen for mainstream primary-school age children. Autism, 6, 9–31.10.1177/136236130200600100311918111]Search in Google Scholar
[Williams, J., Allison, C., Scott, F., Ctott, C., Bolton, P., Baron-Cohen, S., Brayne, S. (2006). The Childhood Asperger Syndrome Test (CAST): Test–retest reliability. Autism, 10, 415–427.10.1177/136236130606661216908483]Search in Google Scholar