Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene()

por Linhares, Natália D., Svartman, Marta, Salgado, Mauro Ivan, Rodrigues, Tatiane C., da Costa, Silvia S., Rosenberg, Carla, Valadares, Eugênia R.
Publicado 2013

Neuropsychiatric and sleep study in autosomal dominant dopa-responsive dystonia

por Alves Júnior, Ailton C., Daker, Maurício V., Machado, Alexei M.C., Luna, Alan S., Valladares Neto, Dirceu C., Valadares, Eugenia R.
Publicado 2022

Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization

por Linhares, Natália D., Valadares, Eugênia R., da Costa, Silvia S., Arantes, Rodrigo R., de Oliveira, Luiz Roberto, Rosenberg, Carla, Vianna-Morgante, Angela M., Svartman, Marta
Publicado 2016

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells

por Ho, Bianca, Greenlaw, Keelin, Al Tuwaijri, Abeer, Moussette, Sanny, Martínez, Francisco, Giorgio, Elisa, Brusco, Alfredo, Ferrero, Giovanni Battista, Linhares, Natália D., Valadares, Eugênia R., Svartman, Marta, Kalscheuer, Vera M., Rodríguez Criado, Germán, Laprise, Catherine, Greenwood, Celia M. T., Naumova, Anna K.
Publicado 2018