Veerle De Wolf

Association of CDH11 with non‐syndromic ASD

H. Peeters, D. Lambrechts, K. Devriendt, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Variability in expression of a familial 2.79 Mb microdeletion in chromosome14q22.1–22.2

K. Devriendt, J. Vermeesch, E. Ortibus, 2012, American journal of medical genetics. Part A.

Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example

H. Peeters, K. Devriendt, N. Brison, 2013, American journal of medical genetics. Part A.

A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism

H. Peeters, K. Devriendt, J. Steyaert, 2014, American journal of medical genetics. Part A.

Narrowing the critical deletion region for autism spectrum disorders on 16p11.2

H. Peeters, K. Devriendt, I. Noens, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Association of CDH11 with non‐syndromic ASD

H. Peeters, D. Lambrechts, K. Devriendt, 2014, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.