Items where authors include "Ockeloen, C.W."

Article

Woods, E. orcid.org/0000-0003-2349-2688, Holmes, N., Denommé‐Pichon, A.S. orcid.org/0000-0002-8986-8222 et al. (14 more authors) (2025) An international ASXL3 natural history study: deep phenotypic analyses including detailed reports of a milder phenotype, novel associations, and clinical recommendations. American Journal of Medical Genetics Part A. e64157. ISSN 1552-4825

Schirwani, S., Woods, E., Koolen, D.A. et al. (8 more authors) (2023) Familial Bainbridge-Ropers syndrome: report of familial ASXL3 inheritance and a milder phenotype. American Journal of Medical Genetics Part A, 191 (1). pp. 29-36. ISSN 1552-4825