Maria R. G. O. Rebouças

Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?

Ágatha Cristhina Oliveira Faria, Eliete Rabbi‐Bortolini, Maria R. G. O. Rebouças et al. · American Journal of Medical Genetics Part A · 2015 · 47 citations

Genetics, Pathology, Disease Gene Identification +24

Mutational characterization of the P3H1/CRTAP/CypB complex in recessive osteogenesis imperfecta

Clara Barbirato, Maíra Trancozo, Marcos Guilherme Melo de Almeida et al. · Genetics and Molecular Research · 2015 · 21 citations · Full text

Osteogenesis imperfecta in Brazilian patients

Maíra Trancozo, Marcos V.D. Moraes, Dalila A. Silva et al. · Genetics and Molecular Biology · 2019 · 18 citations · Full text

Bone Disease, Bone Fragility, Osteopathy +14

A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta

Clara Barbirato, Marcos Guilherme Melo de Almeida, M. Milanez et al. · Genetics and Molecular Research · 2009 · 14 citations · Full text

Bone Disease, Developmental Anomaly, Bone Fragility +14