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The Application of Next-Generation Sequencing for Mutation Detection in Autosomal-Dominant Hereditary Hearing Impairment.
Gürtler, Nicolas; Röthlisberger, Benno; Ludin, Katja; Schlegel, Christoph; Lalwani, Anil K.
Affiliation
  • Gürtler N; *Department of Otolaryngology, University Hospital Basel, Basel †Medical Genetics, Center for Laboratory Medicine, Cantonal Hospital Aarau, Aarau ‡Department of Otolaryngology, Cantonal Hospital Luzern, Luzern, Switzerland §Department of Otolaryngology, Columbia University, New York, New York, USA.
Otol Neurotol ; 38(6): 900-903, 2017 07.
Article in En | MEDLINE | ID: mdl-28419064
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / High-Throughput Nucleotide Sequencing / Hearing Loss, Sensorineural Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: Otol Neurotol Journal subject: NEUROLOGIA / OTORRINOLARINGOLOGIA Year: 2017 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / High-Throughput Nucleotide Sequencing / Hearing Loss, Sensorineural Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: Otol Neurotol Journal subject: NEUROLOGIA / OTORRINOLARINGOLOGIA Year: 2017 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos