Hereditary hearing loss SNP-microarray pilot study
Barbara Vona(Brigham and Women's Hospital), Thomas Haaf(University of Würzburg), Michaela A. H. Hofrichter(University of Würzburg), Wafaa Shehata-Dieler, Jörg Schröder, Indrajit Nanda(Udayana University)
Cited by 15
Related Papers
<scp>DFNB16</scp> is a frequent cause of congenital hearing impairment: implementation of <i><scp>STRC</scp></i> mutation analysis in routine diagnostics
|Clinical Genetics|2013|110
Non-syndromic hearing loss gene identification: A brief history and glimpse into the future
|Molecular and Cellular Probes|2015|109
Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations
|Genetics in Medicine|2014|107
Third Report on Chicken Genes and Chromosomes 2015
|Cytogenetic and Genome Research|2015|97