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

Estudo de família brasileira portadora de deficiência auditiva sensorioneural não-sindrômica com herança mitocondrial

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

Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families

by Mingroni-Netto,Regina C., Pavanello,Rita C.M., Otto,Paulo A., Vianna-Morgante,Angela M.
Published 1997

Premature ovarian failure (POF) in Brazilian fragile X carriers

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

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

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

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

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