William Dobyns
36PUBLICATIONS
193CO-AUTHORS

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Publications (36)
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|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
|Jul 08, 2025
Beyond hearing loss: exploring neurological and neurodevelopmental sequelae in asymptomatic congenital cytomegalovirus infection.Meghan R Swanson, Lauren D Haisley, William B Dobyns
|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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Frequent Collaborators
7 joint publications
Kimberly A Aldinger
4 joint publications
Kshitij Mankad
4 joint publications
Ghayda Mirzaa
4 joint publications
Juliette Piard
3 joint publications
Micheil Innes
3 joint publications
Renske Oegema
3 joint publications
Binnaz Yalcin
3 joint publications
A Taranath
3 joint publications
S V Sudhakar
3 joint publications
C A P F Alves