Monica Proud

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

Journal of Medical Genetics · 2010 · 396 citations

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort

American Journal of Medical Genetics Part A · 2016 · 140 citations