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

Lies H Hoefsloot1, Anne-Françoise Roux, Maria Bitner-Glindzicz

  • 1Department of Human Genetics, Radboud University MC, Nijmegen, the Netherlands.

European Journal of Human Genetics : EJHG
|May 23, 2013
PubMed
Abstract

No abstract available in PubMed .

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