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Virmond, Luiza do Amaral
9
results:
Search for persons
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Online (9)
Mediatypes
Articles (Online) (6)
OpenAccess-fulltext (3)
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1
ELMO2 biallelic pathogenic variants in a patient with gingi..:
Perrone, Eduardo
;
Coelho, Antonio Victor Campos
;
Virmond, Luiza do Amaral
...
American Journal of Medical Genetics Part A. , 2024
Link:
https://doi.org/10.1002/..
?
2
Genomic study of nonsyndromic hearing loss in unaffected in..:
Quaio, Caio Robledo D' Angioli Costa
;
Coelho, Antonio Victor Campos
;
Moura, Livia Maria Silva
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
3
The hospital Israelita Albert Einstein standards for consti..:
Quaio, Caio Robledo D'Angioli Costa
;
Ceroni, José Ricardo Magliocco
;
Pereira, Michele Araújo
...
Human Genomics. 17 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
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4
Clinical and molecular evaluation of 13 Brazilian patients ..:
Perrone, Eduardo
;
Perez, Ana Beatriz Alvarez
;
D'Almeida, Vânia
...
American Journal of Medical Genetics Part A. 185 (2020) 4 - p. 1047-1058 , 2020
Link:
https://doi.org/10.1002/..
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5
Additional file 1 of The hospital Israelita Albert Einstein..:
Caio Robledo D'Angioli Costa Quaio
;
José Ricardo Magliocco Ceroni
;
Michele Araújo Pereira
...
doi:10.6084/m9.figshare.24571866.v1. , 2023
Link:
https://doi.org/10.6084/..
?
6
Genomic study of nonsyndromic hearing loss in unaffected in..:
Caio Robledo D' Angioli Costa Quaio
;
Antonio Victor Campos Coelho
;
Livia Maria Silva Moura
...
https://www.frontiersin.org/articles/10.3389/fgene.2022.921324/full. , 2022
Link:
https://doi.org/10.3389/..
?
7
DataSheet1_Genomic study of nonsyndromic hearing loss in un..:
Caio Robledo D' Angioli Costa Quaio
;
Antonio Victor Campos Coelho
;
Livia Maria Silva Moura
...
doi:10.3389/fgene.2022.921324.s001. , 2022
Link:
https://doi.org/10.3389/..
?
8
A novel variant in the COX15 gene causing a fatal infantile..:
Galvão de Oliveira, Manuella
;
Tengan, Célia
;
Micheletti, Cecília
...
European Journal of Medical Genetics. 64 (2021) 5 - p. 104195 , 2021
Link:
https://doi.org/10.1016/..
?
9
Leigh syndrome in a patient with a novel C12orf65 pathogeni..:
Perrone, Eduardo
;
Cavole, Thiago R.
;
Oliveira, Manuella G.
...
Genetics and Molecular Biology. 43 (2020) 2 - p. , 2020
Link:
https://doi.org/10.1590/..
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