E. M. Olsen, Failure to thrive: the prevalence and concurrence of anthropometric criteria in a general infant population, Archives of Disease in Childhood, vol.92, issue.2, pp.109-123, 2007.
DOI : 10.1136/adc.2005.080333

K. Wang, Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity, Diabetes, vol.59, issue.10, pp.2690-2694, 2010.
DOI : 10.2337/db10-0192

S. Girirajan and E. E. Eichler, Phenotypic variability and genetic susceptibility to genomic disorders, Human Molecular Genetics, vol.19, issue.R2, pp.176-87
DOI : 10.1093/hmg/ddq366

S. Girirajan, A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay, Nature Genetics, vol.316, issue.3, pp.203-212
DOI : 10.1038/ng.534

C. Howald, Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions, Journal of Medical Genetics, vol.43, issue.3, pp.266-73, 2006.
DOI : 10.1136/jmg.2005.034009

D. F. Conrad, Origins and functional impact of copy number variation in the human genome, Nature, vol.36, issue.7289, pp.704-716, 2010.
DOI : 10.1038/nature08516

M. B. First, R. L. Spitzer, and J. B. Williams, Structured Clinical Interview for DSM-IV (SCID-I): Users Guide and Interview, Research Version, Biometrics Research Department, 1995.

B. A. Fernandez, Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder, Journal of Medical Genetics, vol.47, issue.3, 2009.
DOI : 10.1136/jmg.2009.069369

L. A. Weiss, Association between Microdeletion and Microduplication at 16p11.2 and Autism, New England Journal of Medicine, vol.358, issue.7, pp.667-75, 2008.
DOI : 10.1056/NEJMoa075974

URL : http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.205.9518

S. E. Mccarthy, Microduplications of 16p11.2 are associated with schizophrenia, Nature Genetics, vol.140, issue.11, pp.1223-1230, 2009.
DOI : 10.1038/ng.236

M. Shinawi, Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioral problems, dysmorphism, epilepsy, and abnormal head size, J Med Genet, 2009.