Items where authors include "Zarate, Y.A."

Article

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

Zarate, Y.A. orcid.org/0000-0001-8235-6200, Bosanko, K.A., Caffrey, A.R. et al. (45 more authors) (2019) Mutation update for the SATB2 gene. Human Mutation, 40 (8). pp. 1013-1029. ISSN 1059-7794

Zarate, Y.A., Smith-Hicks, C.L., Greene, C. et al. (55 more authors) (2018) Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome. American Journal of Medical Genetics Part A, 176 (4). pp. 925-935. ISSN 1552-4825

Proceedings Paper

Zarate, Y.A., Gambello, M., Pandya, A. et al. (19 more authors) (2018) Phenotype and natural history in 49 individuals with SATB2- associated syndrome. In: American Journal of Medical Genetics Part A. 38th Annual David W. Smith Workshop on Malformations and Morphogenesis, 26-29 Aug 2017, Stowe, VT. Wiley , pp. 1526-1527.