Edi Lúcia Sartorato

Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo et al. · The American Journal of Human Genetics · 2003 · 289 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +9

Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy.

Rita De Gasperi, Miguel A. Gama Sosa, Edi Lúcia Sartorato et al. · PubMed · 1996 · 96 citations

Two cases of Y; autosome translocations: A 45, X male and a clinically trisomy 18 patient

Solange B. Farah, Clarisa F. Ramos, Maricilda Palandi de Mello et al. · American Journal of Medical Genetics · 1994 · 82 citations

Connexin 26 35delG does not represent a mutational hotspot

Caryn R. Rothrock, Alessandra Murgia, Edi Lúcia Sartorato et al. · Human Genetics · 2003 · 54 citations

Molecular Biology, Genetic Mechanism, Molecular Genetics +2

Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness

Vânia Belintani Piatto, Eny Maria Goloni‐Bertollo, Edi Lúcia Sartorato et al. · Hearing Research · 2004 · 42 citations

Brazilian Patients, Genetic Disorder, Genetics +8