M. T. Auricchio

Multilocus Family-Based Association Analysis of Seven Candidate Polymorphisms with Essential Hypertension in an African-Derived Semi-Isolated Brazilian Population

A. Pereira, A. C. Pereira, R. Mingroni-Netto, 2012, International journal of hypertension.

Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes.

R. Kleta, Simona Dumitriu, R. Coletta, 2017, Oral surgery, oral medicine, oral pathology and oral radiology.

Multilocus Analyses of Seven Candidate Genes Suggest Interacting Pathways for Obesity‐Related Traits in Brazilian Populations

Mara H. Hutz, M. Hutz, A. Pereira, 2011, Obesity.

Polymorphic Alu insertions in six Brazilian African‐derived populations

P. Otto, R. Mingroni-Netto, M. T. Auricchio, 2004, American journal of human biology : the official journal of the Human Biology Council.

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

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

Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant

J. Mazzeu, P. Otto, R. Mingroni-Netto, 2006 .

Heterogeneous Distribution of HbS and HbC Alleles in Afro-derived Brazilian Populations

A. Barbosa, M. N. Klautau-Guimarães, Í. Ferrari, 2002 .

Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations.

K. Hill, A. Hurtado, F. Salzano, 2002, American journal of medical genetics.

Genomic copy number alterations in non‐syndromic hearing loss

C. Rosenberg, A. Krepischi, S. Costa, 2015, Clinical genetics.

Chromosome imbalances in syndromic hearing loss

J. Mazzeu, A. Vianna-Morgante, C. Rosenberg, 2009, Clinical genetics.