Isabella Lopes Monlleó (Isabella L Monlleó, Isabella Monlleo)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Venues

Genes

Congenital anomalies

American journal of medical genetics. Part C, Seminars in medical genetics

Italian journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 15 (4) (2024)
Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 15 (4) (2024)
Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno, Chong Ae Kim, Elaine Lustosa Mendes, Erlane Marques Ribeiro, Amanda Oliveira, Têmis Maria Félix, Agnes Cristina Fett-Conte, Luciana Cardoso Bonadia, Gabriela Roldão Correia-Costa, Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes, Társis Antonio Paiva Vieira
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity. Genes 15 (4) (2024)
Reinaldo Luna de Omena Filho, Reginaldo José Petroli, Fernanda Caroline Soardi, Débora de Paula Michelatto, Taís Nitsch Mazzola, Helena Fabbri-Scallet, Maricilda Palandi de Mello, Susane Vasconcelos Zanotti, Ida Cristina Gubert, Isabella Lopes Monlleó
So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity. Italian journal of pediatrics 48 (1) (2022)
Luna Lira Bergamini, Samira Spineli-Silva, Têmis Maria Félix, Vera L Gil-da-Silva-Lopes, Tarsis P Vieira, Erlane Marques Ribeiro, Ana Carolina Xavier, Elaine Lustosa-Mendes, Marshall Ítalo Barros Fontes, Isabella Lopes Monlleó
Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases. Congenital anomalies 61 (5) (2021)
Vera Lúcia Gil-da-Silva-Lopes, Milena Atique Tacla, Ilária Cristina Sgardioli, Társis Antonio Paiva Vieira, Isabella Lopes Monlleó
Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 184 (4) (2020)

Isabella Lopes Monlleó.css-eqlu8i{font-size:small;padding-left:4px;} (Isabella L Monlleó, Isabella Monlleo)

Publication Activity (10 Years)

Top Topics

Top Venues

Isabella Lopes Monlleó (Isabella L Monlleó, Isabella Monlleo)