Matheus de Mello Copelli

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 4

Top Topics

Intellectual Disability

Systematic Review

Gene Expression

Top Venues

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

Publications

Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)
Matheus de Mello Copelli, Eleonore Pairet, Milena Atique Tacla, Társis Antonio Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
SATB2 -Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 14 (4) (2023)