R. S. Abreu-Silva

Prevalence of GJB 2 ( Connexin-26 ) and GJB 6 ( Connexin-30 ) Mutations in a Cohort of 300 Brazilian Hearing-Impaired Individuals : Implications for Diagnosis and Genetic Counseling

P. Otto, R. Mingroni-Netto, A. C. Batissoco, 2008 .

Novel OTOF mutations in Brazilian patients with auditory neuropathy

J. Romanos, R. Mingroni-Netto, L. Kimura, 2009, Journal of Human Genetics.

Is autosomal recessive deafness associated with oculocutaneous albinism a “coincidence syndrome”?

R. Mingroni-Netto, Eliete Pardono, A. C. Batissoco, 2006, Journal of Human Genetics.

The search of a genetic basis for noise-induced hearing loss (NIHL)

A. Horimoto, P. Otto, R. Mingroni-Netto, 2011, Annals of human biology.

Prevalence of GJB2 (Connexin-26) and GJB6 (Connexin-30) Mutations in a Cohort of 300 Brazilian Hearing-Impaired Individuals: Implications for Diagnosis and Genetic Counseling

P. Otto, R. Mingroni-Netto, Ana Carla Batissoco, 2009, Ear and hearing.

Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients.

P. Otto, R. Mingroni-Netto, Karina Lezirovitz, 2006, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness

J. Romanos, R. Mingroni-Netto, Eliete Pardono, 2008, European Journal of Human Genetics.

Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness

J. Romanos, R. Mingroni-Netto, Eliete Pardono, 2008, European Journal of Human Genetics.