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EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus
Journal article   Peer reviewed

EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus

Lies Hoefsloot, Anne-Françoise Roux and Maria Bitner-Glindzicz
European Journal of Human Genetics, Vol.21(11), pp.1325-1329
11/2013
PMCID: PMC3798855
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