Fernanda Borchers Coeli

Matrix metalloproteinase 9 gene haplotypes affect left ventricular hypertrophy in hypertensive patients

Riccardo Lacchini, Anna L. Jacob‐Ferreira, Marcelo R. Luizon et al. · Clinica Chimica Acta · 2010 · 43 citations

Medicine, Cardiology, Genetics +15

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

46,XX Male - Testicular Disorder of Sexual Differentiation (DSD): hormonal, molecular and cytogenetic studies

Crésio Alves, Zilda Braid, Fernanda Borchers Coeli et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 2010 · 23 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Novel deletion alleles carrying CYP21A1P/A2chimeric genes in Brazilian patients with 21-hydroxylase deficiency

Fernanda Borchers Coeli, Fernanda Caroline Soardi, R.D. Bernardi et al. · BMC Medical Genetics · 2010 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Complete XY gonadal dysgenesis due to p.D293N homozygous mutation in theNR5A1 gene: a case study

Fernanda Caroline Soardi, Fernanda Borchers Coeli, Andréa Trevas Maciel‐Guerra et al. · Journal of Applied Genetics · 2010 · 22 citations

Life Sciences, Genetics, Molecular Genetics +14