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F. A. R. Madia
F. A. R. Madia
University of São Paulo
Medicine
Microcephaly
Cri du chat
Breakpoint
Genetics
4
Papers
1
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0
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Investigating the CNVs in routine diagnostics using WES and array in Brazilian patients
2019
Evelin Aline Zanardo
Samar N. Chehimi
Fabíola Paoli Monteiro
F. A. R. Madia
Gil M. Novo-Filho
Alexandre T. Dias
Marília M. Montenegro
Y. G. Oliveira
L. L. Vieira
Mariana Vilela Rocha
A. S. Brasil
Amom M. Nascimento
Thais V. M. M. Costa
J. G. Damasceno
Fernando Kok
Chong Ae Kim
Leslie Domenici Kulikowski
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Breakpoint delineation in 5p‐ patients leads to new insights about microcephaly and the typical high‐pitched cry
2019
Molecular Genetics & Genomic Medicine
Samar N. Chehimi
Evelin Aline Zanardo
José Ricardo Magliocco Ceroni
Amom M. Nascimento
F. A. R. Madia
Alexandre T. Dias
Gil Monteiro Novo Filho
Marília M. Montenegro
J. G. Damasceno
Thais V. M. M. Costa
Yanca Gasparini
Chong Ae Kim
Leslie Domenici Kulikowski
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Multi-gene panel testing improves diagnosis in Brazilian patients with Early-Onset Epilepsy
2019
G. M. Novo Filho
Alexandre T. Dias
Amom M. Nascimento
J. G. Damasceno
Evelin Aline Zanardo
Samar N. Chehimi
F. A. R. Madia
O. S. Akl
Marília M. Montenegro
Y. G. Oliveira
L. L. Vieira
M.L.G. Manreza
Leslie Domenici Kulikowski
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Molecular autopsy reveals clues for genetic basis of congenital valve defect
2019
F. A. R. Madia
Alexandre T. Dias
Evelin Aline Zanardo
J. G. Damasceno
Amom M. Nascimento
Thais V. M. M. Costa
Samar N. Chehimi
Gil M. Novo-Filho
Marília M. Montenegro
Y. G. Oliveira
A.B. Freitas
L. L. Vieira
Regina Schultz
Fernanda de Toledo Gonçalves
Cintia Fridman
Chong Ae Kim
Leslie Domenici Kulikowski
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