Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR, and Rodier PM. Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders. Teratology, 62:393-405, 2000.

Smith M, Filipek PA, Wu C, Bocian M., Hakim S, Modahl C, and Spence MA. Analysis of a 1-megabase deletion i9n 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q23 and 15q11-q13. American Journal of Medical Genetics (Neuropsychiatric Genetics), 96:765-770, 2000.

Instituto Nacional de Salud Infantil y Desarrollo Humano

NIH Pub. No. 01-4961(S) abril 2002

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