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Medrxiv : the Preprint Server for Health Sciences|July 23, 2024
Development and validation of a stakeholder-driven, self-contained electronic informed consent platform for trio-based genomic research studiesBethany Y Norton, James Liu, Sara A Lewis, et al.
Nature Genetics|September 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsySheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, et al.
American Journal of Human Genetics|October 9, 2021
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing lossElodie M Richard, Somayeh Bakhtiari, Ashley P L Marsh, et al.
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