The name is absent

Autism prodrome 64 of 89

expressed in brain yet are subject to epigenetic dysregulation in autism-
spectrum disorders. Human Molecular Genetics, 16, 691-703.

Horike, S., Cai, S., Miyano, M., Cheng, J. F., & Kohwi-Shigematsu, T. (2005).

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett
syndrome. Nature Genetics, 37, 31-40.

Hultman, C., Sparen, P., & Cnattingius, S. (2002). Perinatal risk factors for
infantile autism. Epidemiology, 13, 417-423.

Hurley, R. S., Losh, M., Parlier, M., Reznick, J. S., & Piven, J. (2007). The
broad autism phenotype questionnaire. Journal of Autism and Developmental
Disorders, 37, 1679-1690.

Jamain, S., Quach, H., Betancur, C., Rastam, M., Colineaux, C., Gillberg, I. C.,
et al. (2003). Mutations of the X-linked genes encoding neuroligins NLGN3
and NLGN4 are associated with autism. Nature Genetics, 34, 27-29.

Jiang, Y. H., Sahoo, T., Michaelis, R. C., Bercovich, D., Bressler, J., Kashork,
C. D., et al. (2004). A mixed epigenetic/genetic model for oligogenic
inheritance of autism with a limited role for UBE3A. American Journal of
Medical Genetics Part A, 131, 1-10.

Johnson, C. P. (2004). New tool helps physicians diagnose autism early. AAP
News, 24, 74.

Johnson, C. P, Myers, S. M. and the Council on Children with Disabilities
(2007). Identification and evaluation of children with Autism Spectrum
Disorders. Pediatrics, 120, 1183-1215.

Just, M., Cherkassky, V., Keller, T., Kana, R., & Minshew, N. (2007).

Functional and anatomical cortical underconnectivity in autism: evidence

<<   61   62   63   64   65   66   67   >>

More intriguing information