Flávia Leme de Calais

The novel p.Cys65Tyr mutation in NR5A1gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency

Helena Fabbri‐Scallet, Juliana Gabriel Ribeiro de Andrade, Fernanda Caroline Soardi et al. · BMC Medical Genetics · 2014 · 40 citations · Full text

Medicine, Endocrinology, Genetics +17

Clinical and molecular spectrum of patients with 17β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency

Carla Cristina Telles de Sousa Castro, Guilherme Guaragna‐Filho, Flávia Leme de Calais et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 2012 · 37 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5<i>α</i>-Reductase Type 2 Deficiency

Nélio Neves Veiga-Junior, Pedro Augusto Rodrigues Medaets, Reginaldo José Petroli et al. · International Journal of Endocrinology · 2011 · 32 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Novel splice‐switching oligonucleotide promotes <i>BRCA1</i> aberrant splicing and susceptibility to PARP inhibitor action

Lindsay Smith, Flávia Leme de Calais, Michela Raponi et al. · International Journal of Cancer · 2016 · 21 citations · Full text

Life Sciences, Molecular Biology, Oncology +15

Severe forms of partial androgen insensitivity syndrome due to p.L830F novel mutation in androgen receptor gene in a Brazilian family

Reginaldo José Petroli, Andréa Trevas Maciel‐Guerra, Fernanda Caroline Soardi et al. · BMC Research Notes · 2011 · 12 citations · Full text

Medicine, Genetics, Molecular Genetics +17