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University Center for Excellence in Developmental Disabilities
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  2. 2021

2021

Rapid transition to telemedicine during the COVID-19 pandemic: Medical genetics experience.

6 feet apart but working together.

Otolaryngology utilization in patients with achondroplasia: Results from the CLARITY study.

Multidisciplinary care of neurosurgical patients with genetic syndromes.

Early identification of autism spectrum disorder among children aged 4 years – autism and developmental disabilities monitoring network, 11 sites, United States, 2018.

Translating molecular technologies into routine newborn screening practice.

Is FMR1 CGG repeat number polymorphism associated with phenotypic variation in the general population?

Mild neurological signs in FMR1 premutation women in an unselected community-based cohort.

Educational interventions for children and youth with autism: A 40-year perspective.

Stress and genetics influence hair cortisol in FMR1 premutation carrier mothers of children with fragile X syndrome.

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