Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.

Autor: Jacquemont, M.-l., Sanlaville, D., Redon, R., Raoul, O., Cormier-Daire, V., Lyonnet, S., Amiel, J., Le Merrer, M., Heron, D., De Blois, M.-C., Prieur, M., Vekemans, M., Carter, N. P., Munnich, A., Colleaux, I., Philippe, A.

Publikováno v: Journal of Medical Genetics; Nov2006, Vol. 43 Issue 11, p843-849, 7p, 1 Black and White Photograph, 3 Charts, 1 Graph