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

被引：0
|
作者：
Lies H Hoefsloot
Anne-Françoise Roux
Maria Bitner-Glindzicz
机构：
[1] Radboud University MC,Department of Human Genetics
[2] CHU Montpellier,undefined
[3] Laboratoire de Génétique Moléculaire,undefined
[4] Inserm,undefined
[5] U827,undefined
[6] Univ Montpellier I,undefined
[7] Clinical and Molecular Genetics Unit,undefined
[8] Institute of Child Health,undefined
[9] UCL,undefined
来源：
European Journal of Human Genetics | 2013年 / 21卷
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页码：1325 / 1329
页数：4
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