[HTML][HTML] Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
SCS Carvalho, CHP Grangeiro… - BMC Research …, 2018 - Springer
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
CHP Grangeiro, CG Picanco-Albuquerque… - BMC Research …, 2018 - go.gale.com
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
E Simone da Costa, CHP Grangeiro… - BMC research …, 2018 - pubmed.ncbi.nlm.nih.gov
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort.
C SDCES, CHP Grangeiro… - BMC Research …, 2018 - europepmc.org
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
[HTML][HTML] Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
CHP Grangeiro, CG Picanço-Albuquerque… - BMC Research …, 2018 - ncbi.nlm.nih.gov
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
CHP Grangeiro, CG Picanço-Albuquerque… - BMC Research …, 2018 - search.proquest.com
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort.
CHP Grangeiro… - BMC Research …, 2018 - search.ebscohost.com
Objective: Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
CHP Grangeiro, CG Picanço-Albuquerque… - 2018 - agris.fao.org
Objective Hereditary hearing loss (HL) is the most common sensorineural disorder in
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
humans. Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 …
[HTML][HTML] Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
CHP Grangeiro… - BMC …, 2018 - bmcresnotes.biomedcentral.com
Hereditary hearing loss (HL) is the most common sensorineural disorder in humans.
Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 gene …
Besides mutations in GJB2 and GJB6 genes, pathogenic variants in the SLC26A4 gene …
[引用][C] Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
SC Carvalho, CHP Grangeiro… - BMC Research …, 2018 - repositorio.usp.br
ReP USP - Detalhe do registro: Contribution of SLC26A4 to the molecular diagnosis of
nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort Home About USP …
nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort Home About USP …