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Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform.
De Keulenaer, Sarah; Hellemans, Jan; Lefever, Steve; Renard, Jean-Pierre; De Schrijver, Joachim; Van de Voorde, Hendrik; Tabatabaiefar, Mohammad Amin; Van Nieuwerburgh, Filip; Flamez, Daisy; Pattyn, Filip; Scharlaken, Bieke; Deforce, Dieter; Bekaert, Sofie; Van Criekinge, Wim; Vandesompele, Jo; Van Camp, Guy; Coucke, Paul.
Affiliation
  • De Keulenaer S; NXTGNT, Ghent University, Ghent, Belgium.
BMC Med Genomics ; 5: 17, 2012 May 18.
Article in En | MEDLINE | ID: mdl-22607986
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Molecular Diagnostic Techniques / Deafness / High-Throughput Nucleotide Sequencing Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: BMC Med Genomics Journal subject: GENETICA MEDICA Year: 2012 Document type: Article Affiliation country: Belgium Country of publication: United kingdom
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Molecular Diagnostic Techniques / Deafness / High-Throughput Nucleotide Sequencing Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: BMC Med Genomics Journal subject: GENETICA MEDICA Year: 2012 Document type: Article Affiliation country: Belgium Country of publication: United kingdom