Items where authors include "Pierson, T.M."

Article

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

Zarate, Y.A., Bosanko, K.A., Thomas, M.A. et al. (18 more authors) (2021) Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Clinical Genetics, 99 (4). pp. 547-557. ISSN 0009-9163