Milena Atique Tacla (Milena Atique-Tacla)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Topics

Intellectual Disability

Fluorescent Probe

Top Venues

European journal of human genetics : EJHG

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

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)
Milena Atique Tacla, Matheus de Mello Copelli, Eleonore Pairet, Isabella Lopes Monlleó, Erlane Marques Ribeiro, Elaine Lustosa Mendes, Raphaël Helaers, Társis Antonio Paiva Vieira, Miikka Vikkula, Vera Lúcia Gil-da-Silva-Lopes
Molecular investigation in individuals with orofacial clefts and microphthalmia-anophthalmia-coloboma spectrum. European journal of human genetics : EJHG (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)
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)