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Lucas Vieira Lacerda Pires

University of São Paulo

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Atypical, severe hypertrophic cardiomyopathy in a newborn presenting Noonan syndrome harboring a recurrent heterozygous MRAS variant.

2021 American Journal of Medical Genetics Part A
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Nationwide questionnaire data of 229 Williams-Beuren syndrome patients using WhatsApp tool.

2021 Arquivos De Neuro-psiquiatria
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Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms

2021 Clinical Genetics
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