Cargando…
Genetics of Deafness
Autores principales: | Sartorato, Edi Lúcia, Friderici, Karen, Del Castillo, Ignacio |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337585/ https://www.ncbi.nlm.nih.gov/pubmed/22567392 http://dx.doi.org/10.1155/2012/562848 |
Ejemplares similares
-
Molecular genetics of non-syndromic deafness
por: Piatto, Vânia B., et al.
Publicado: (2015) -
A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene
por: Martins, Fábio Tadeu Arrojo, et al.
Publicado: (2018) -
Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping Platform
por: Martins, Fábio Tadeu Arrojo, et al.
Publicado: (2013) -
Advances in Molecular Genetics and the Molecular Biology of Deafness
por: Nishio, Shin-ya, et al.
Publicado: (2016) -
Deaf-Mutes
Publicado: (1896)