“Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion”

Researchers at the University of Chicago have completed a study which “suggests that the 22q13 deletion phenotype includes abnormal posterior fossa structures that are unlikely to be attributed to SHANK3 disruption.” This study also indicates other genes which may be related 22q13.3 deletion phenotypes. To read more, click here.

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