Isabella Monlleo
4PUBLICATIONS
6CO-AUTHORS
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Publications (4)
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|Apr 27, 2024
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno
|Jun 10, 2022
So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity.Reinaldo Luna de Omena Filho, Reginaldo José Petroli, Fernanda Caroline Soardi
|Apr 26, 2021
Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases.Luna Lira Bergamini, Samira Spineli-Silva, Têmis Maria Félix
|Nov 09, 2020
Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome.Vera Lúcia Gil-da-Silva-Lopes, Milena Atique Tacla, Ilária Cristina Sgardioli
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