EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus - Université de Montpellier Accéder directement au contenu
Article Dans Une Revue European Journal of Human Genetics Année : 2013

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hal-02446172 , version 1 (20-01-2020)

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Lies Hoefsloot, Anne-Françoise Roux, Maria Bitner-Glindzicz. EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus. European Journal of Human Genetics, 2013, 21 (11), pp.1325-1329. ⟨10.1038/ejhg.2013.83⟩. ⟨hal-02446172⟩
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