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Bita Hashemi

University of Toronto

4

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X-linked Joubert syndrome: Neuroimaging and clinical features associated with a novel mutation in oral-facial-digital syndrome type 1

2015 Journal of pediatric neurology
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Deletion of 15q11.2(BP1‐BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population

2015 American Journal of Medical Genetics Part A
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CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

2014 Journal of Neurodevelopmental Disorders
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