TY  - GEN
AU  - Cabanillas, Ruben
AU  - Dineiro, Marta
AU  - Cifuentes, Guadalupe A
AU  - Castillo, David
AU  - Pruneda, Patricia C
AU  - Alvarez, Rebeca
AU  - Sanchez-Duran, Noelia
AU  - Capin, Raquel
AU  - Plasencia, Ana
AU  - Viejo-Diaz, Monica
AU  - Garcia-Gonzalez, Noelia
AU  - Hernando, Ines
AU  - Llorente, Jose L
AU  - Reparaz-Andrade, Alfredo
AU  - Torreira-Banzas, Cristina
AU  - Rosell-Andreo, Jordi
AU  - Govea-Callizo, Nancy
AU  - Ramon Gomez-Martinez, Justo
AU  - Nunez-Batalla, Faustino
AU  - Garrote, Jose A
AU  - Mazon-Gutierrez, Angel
AU  - Costales, Maria
AU  - Isidoro-Garcia, Maria
AU  - Garcia-Berrocal, Belen
AU  - Ordonez, Gonzalo R
AU  - Cadinanos, Juan
PY  - 2018
DO  - 10.1186/s12920-018-0375-5
UR  - https://hdl.handle.net/20.500.12105/22547
AB  - Background: Sensorineural hearing loss (SNHL) is the most common sensory impairment. Comprehensive next-generation sequencing (NGS) has become the standard for the etiological diagnosis of early-onset SNHL. However, accurate selection of target...
LA  - eng
PB  - BioMed Central (BMC)
KW  - Hereditary
KW  - Hearing loss
KW  - Precision
KW  - Diagnostics
KW  - NGS
KW  - Gene panel
KW  - Child
KW  - Young Adult
KW  - Spain
KW  - Adult
KW  - Hearing Loss
KW  - Humans
KW  - Child, Preschool
KW  - Adolescent
KW  - Middle Aged
KW  - Infant
KW  - Phenotype
KW  - Male
KW  - Infant, Newborn
KW  - Female
KW  - Genomics
KW  - High-Throughput Nucleotide Sequencing
KW  - INDEL Mutation
TI  - Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
TY  - research article
ER  -