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Results 1-4 of 4 (Search time: 0.046 seconds).
| Issue Date | Title | Author(s) |
|---|---|---|
| 2022 | Genetic etiology of non-syndromic hearing loss in Latin America (Oct, 10.1007/s00439-021-02354-4, 2021) | LEZIROVITZ, Karina; MINGRONI-NETTO, Regina Celia |
| 2022 | Frequency and origin of the c.2090T > G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss | BUENO, Andre S.; NUNES, Kelly; DIAS, Alex M. M.; ALVES, Leandro U.; MENDES, Beatriz C. A.; SAMPAIO-SILVA, Juliana; SMITS, Jeroen; YNTEMA, Helger G.; MEYER, Diogo; LEZIROVITZ, Karina; MINGRONI-NETTO, Regina C. |
| 2022 | NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss (vol 29, pg 3691, 2020) | SALAZAR-SILVA, R.; DANTAS, Vitor Lima Goes; ALVES, Leandro Ucela; BATISSOCO, Ana Carla; OITICICA, Jeanne; LAWRENCE, Elizabeth A.; KAWAFI, Abdelwahab; YANG, Yushi; NICASTRO, Fernanda Stavale; NOVAES, Beatriz Caiuby; HAMMOND, Chrissy; KAGUE, Erika; MINGRONI-NETTO, R. C. |
| 2022 | New Insights into the Identity of the DFNA58 Gene | NASCIMENTO, Larissa Reis do; VIEIRA-SILVA, Gleiciele Alice; KITAJIMA, Joao Paulo Fumio Whitaker; BATISSOCO, Ana Carla; LEZIROVITZ, Karina |
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