William Dobyns

36PUBLICATIONS
193CO-AUTHORS
Genome structure and regulationNeurology and neuromuscular diseasesNeonatologyInfant and child healthHypersonic propulsion and hypersonic aerothermodynamics
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Publications (36)

|Nov 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Ghayda M Mirzaa, Keqin Yan, Raissa Relator

|Sep 12, 2025
Pontocerebellar hypoplasia: a review from 1912 to 2022.

Natalie A Kukulka, Shriya Singh, Matthew T Whitehead

|May 03, 2025
Further Delineation of the AUTS2 HX Repeat Domain-Related Phenotype.

Esin Nur Erdogan, Chi Vicky Cheng, Stefano G Caraffi

|Oct 25, 2024
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations.

Angela Peron, Felice D'Arco, Kimberly A Aldinger

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