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

Article

Low, K.J. orcid.org/0000-0002-4975-9363, Foreman, J., Hobson, R.J. orcid.org/0000-0003-1997-9557 et al. (13 more authors) (2025) The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disorders. European Journal of Human Genetics. ISSN 1018-4813

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