Isabella Monlleo

5PUBLICATIONS
35CO-AUTHORS
Respiratory diseasesDevelopmental genetics (incl. sex determination)Cancer diagnosis
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Publications (5)

|Sep 15, 2026
Rare diseases in Brazil: a nationwide analysis of the diagnostic odyssey.

|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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Frequent Collaborators

2 joint publications

Vera Lúcia Gil-da-Silva-Lopes

2 joint publications

Társis Paiva Vieira

2 joint publications

Chong Ae Kim

1 joint publications

Milena Atique Tacla