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Scientific Reports|September 8, 2018
A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual DisabilityJ R M Ceroni, R L Dutra, R S Honjo, et al.
Molecular Genetics and Metabolism|October 16, 2013
Mucopolysaccharidosis type II: identification of 30 novel mutations among Latin American patientsA C Brusius-Facchin, I V D Schwartz, C Zimmer, et al.
Journal of Inherited Metabolic Disease|October 13, 2009
Clinical and biochemical studies in mucopolysaccharidosis type II carriersI V D Schwartz, L L C Pinto, G Breda, et al.
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