1 Laboratoire de Génétique Moléculaire Humaine, Faculté de Médecine, 3018 Sfax, Tunisia 2 Unité de Génétique Epidémiologique, Faculté de Médecine, 1007 Tunis, Tunisia So far, no distinctive clinical ...
Non-syndromic hearing impairment is one of the most heterogeneous hereditary conditions, with more than 40 reported gene localisations. We have identified a large Dutch family with autosomal dominant ...
2 Unidad de Investigación Medica, HG CMN La Raza, IMSS, Mexico Correspondence to: Dr K Jáuregui-Renaud Unidad de Investigación Medica, HG Centro Medico Nacional La Raza, IMSS, Av Vallejo y Jacarandas ...
The latest figures from the Scottish Government indicate around 850,000 people in Scotland are living with some form of hearing loss and of those, 70 per cent are over 70 - some 595,000. Across Great ...
Introduction A meta-analysis of published articles is usually done using standard scales and checklists. Several such scales and checklists are reported in the literature. However, there is little ...
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