Fabricia Andreia Rosa Madia (Fabrícia A R Madia)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 4

Top Topics

Peripheral Blood

Genome Wide Identification

Top Venues

BMC research notes

Molecular genetics & genomic medicine

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

Publications

Márcia Regina Gimenes Adriano, Adriana Bortolai, Fabricia Andreia Rosa Madia, Gleyson Francisco da Silva Carvalho, Amom Mendes Nascimento, Evelin Aline Zanardo, Beatriz Martins Wolff, Jaques Waisberg, Adriana Bos-Mikich, Leslie Domenici Kulikowski, Alexandre Torchio Dias
Cytogenetics investigation in 151 Brazilian infertile male patients and genomic analysis in selected cases: experience of 14 years in a public genetic service. BMC research notes 17 (1) (2024)
Márcia Regina Gimenes Adriano, Adriana Bortolai, Fabricia Andreia Rosa Madia, Gleyson Francisco da Silva Carvalho, Amom Mendes Nascimento, Evelin Aline Zanardo, Beatriz Martins Wolff, Jaques Waisberg, Adriana Bos-Mikich, Leslie Domenici Kulikowski, Alexandre Torchio Dias
Cytogenetics investigation in 151 Brazilian infertile male patients and genomic analysis in selected cases: experience of 14 years in a public genetic service. BMC research notes 17 (1) (2024)
Márcia Regina Gimenes Adriano, Adriana Bortolai, Fabricia Andreia Rosa Madia, Gleyson Francisco da Silva Carvalho, Amom Mendes Nascimento, Evelin Aline Zanardo, Beatriz Martins Wolff, Jaques Waisberg, Adriana Bos-Mikich, Leslie Domenici Kulikowski, Alexandre Torchio Dias
Cytogenetics investigation in 151 Brazilian infertile male patients and genomic analysis in selected cases: experience of 14 years in a public genetic service. BMC research notes 17 (1) (2024)
Samar N Chehimi, Evelin Aline Zanardo, José Ricardo Magliocco Ceroni, Amom Mendes Nascimento, Fabricia Andreia Rosa Madia, Alexandre Torchio Dias, Gil M N Filho, Marília M Montenegro, Jullian Gabriel Damasceno, Thaís V M M Costa, Yanca Gasparini, Chong Ae Kim, Leslie Domenici Kulikowski
Breakpoint delineation in 5p- patients leads to new insights about microcephaly and the typical high-pitched cry. Molecular genetics & genomic medicine 8 (2) (2019)