35 documents found, page 1 of 4
Corrigendum to: NCOA3 identified as a new candidate to explain autosomal domina...
Mingroni-Netto, Regina Célia
Correction to: genetic etiology of non-syndromic hearing loss in Latin America
Mingroni-Netto, Regina Célia
Genetic etiology of non-syndromic hearing loss in Latin America
Mingroni-Netto, Regina Célia
Whole-genome sequencing of 1,171 elderly admixed individuals from São Paulo, Br...
Naslavsky, Michel S.; Scliar, Marilia O.; Yamamoto, Guilherme L.; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, KellyMade available in DSpace on 2022-04-29T08:46:40Z (GMT). No. of bitstreams: 0 Previous issue date: 2022-12-01; National Institute of General Medical Sciences; As whole-genome sequencing (WGS) becomes the gold standard tool for studying population genomics and medical applications, data on diverse non-European and admixed individuals are still scarce. Here, we present a high-coverage WGS dataset of 1,171 highly a...
NCOA3 identified as a new candidate to explain autosomal dominant progressive h...
Mingroni-Netto, Regina Célia
Further evidence for loss-of-function mutations in the CEACAM16 gene causing no...
Mingroni-Netto, Regina Célia
Aconselhamento genético: será que eu preciso?
Mingroni-Netto, Regina Célia
Waardenburg syndrome: novel mutations in a large Brazilian
Mingroni-Netto, Regina Célia
Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- i...
Mingroni-Netto, Regina Célia
Branco pelo lado paterno, negro pelo materno. [Depoimento a Peter Moon]
Mingroni-Netto, Regina Célia