Buscar

Mostrando ítems 1-8 de 8

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

Dantas, Vítor de Góes Lima; Mandelbaum, Karina Lezirovitz; Yamamoto, Guilherme Lopes; Souza, Carolina Fischinger Moura de; Ferreira, Simone Gomes; Netto, Regina Celia Mingroni (Sociedade Brasileira de Genética - SBGRibeirão Preto, 2014-11-14)

We studied a family presenting 10 individuals affected by autosomal dominant deafness in all frequencies and three individuals affected by high frequency hearing loss. Genomic scanning using the 50k Affymetrix microarray ...

Molecular Genetics Of Non-syndromic Deafness [genética Molecular Da Deficiência Auditiva Não-sindrômica]

Piatto V.B.; Nascimento E.C.T.; Alexandrino F.; Oliveira C.A.; Lopes A.C.P.; Sartorato E.L.; Maniglia J.V. (, 2005)

Rol de los canales Kv7.4 en la sordera de progresión lenta DFNA2

Carignano, Camila (2023)

Características epidemiológicas dos óbitos fetais e neonatais precoces de filhos de pacientes com near mis

Nardello, Daniele Marin (Universidade Federal de SergipePós-Graduação em EnfermagemBrasilUFS, 2017)

Gasdermin E suppresses tumour growth by activating anti-tumour immunity

Zhang, Zhibin; Zhang, Ying; Xia, Shiyu; Kong, Qing; Li, Shunying; Liu, Xing; Junqueira, Caroline; Meza-Sosa, Karla F; Mok, Temy Mo Yin; Ansara, James; Sengupta, Satyaki; Yao, Yandan; Wu, Hao; Lieberman, Judy (Nature Publishing Group, 2023)

Estudo genético de perdas auditivas hereditárias mediante novas tecnologias baseadas em array-CGH e next-generation sequencingGenetic study of hereditary hearing loss with new technologies based on array-CGH and next-generation sequencing

Ramos, Priscila Zonzini, 1987- ([s.n.], 2016)

Genetic Investigation Of Non-syndromic Hereditary Deafness [a Investigação Genética Na Surdez Hereditária Não-sindrômica]

Pfeilsticker L.N.; Stole G.; Sartorato E.L.; Delfino D.; Guerra A.T.M. (, 2004)

Optimization Of Simultaneous Screening Of The Main Mutations Involved In Non-syndromic Deafness Using The Taqman® Openarray™ Genotyping Platform

Martins F.T.A.; Ramos P.Z.; Svidnicki M.C.C.M.; Castilho A.M.; Sartorato E.L. (, 2013)