Structure and stability upon maternal transmission of common and intermediate FMR1 (Fragile X Mental Retardation 1) alleles in a sample of the Brazilian population

by Leonardo P. Capelli, Regina C. Mingroni-Netto, Angela M. Vianna-Morgante
Published 2005-03-01

Study of a Brazilian Family Presenting Non-syndromic hearing loss with mitochondrial inheritance

by Altair Cadrobbi Pupo, Sulene Pirana, Mauro Spinelli, Karina Lezirovitz, Regina C. Mingroni Netto, Lisandra S. Macedo
Published 2008-09-01

A Cell Junctional Protein Network Associated with Connexin-26

by Ana C. Batissoco, Rodrigo Salazar-Silva, Jeanne Oiticica, Ricardo F. Bento, Regina C. Mingroni-Netto, Luciana A. Haddad
Published 2018-08-01

Premature ovarian failure (POF) in Brazilian fragile X carriers

by Angela M. Vianna-Morgante, Silvia S. Costa, Rita de C.M. Pavanello, P.A. Otto, Regina C. Mingroni-Netto
Published 1999-12-01

Inbreeding estimates in human populations: Applying new approaches to an admixed Brazilian isolate.

by Renan B Lemes, Kelly Nunes, Juliana E P Carnavalli, Lilian Kimura, Regina C Mingroni-Netto, Diogo Meyer, Paulo A Otto
Published 2018-01-01

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family

by Vitor G.L. Dantas, Karina Lezirovitz, Guilherme L. Yamamoto, Carolina Fischinger Moura de Souza, Simone Gomes Ferreira, Regina C. Mingroni-Netto
Published 2014-12-01

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

by Eliete Pardono, Juliana F. Mazzeu, Karina Lezirovitz, Maria Teresa B.M. Auricchio, Paula Iughetti, Rafaella M.P. Nascimento, Regina C. Mingroni-Netto, Paulo A. Otto
Published 2006-01-01