Genetic Testing and Molecular Biomarkers · 2011 · 13 citations · 20 references
Our study suggests a need for detecting the carriers. This is the first step for the construction of a national database and provides information for health planners and policy makers to help them in planning programs and allocation resources. The molecular testing was well received by pregnant women and appears to be feasible and highly acceptable.
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Connexin-26 mutations in sporadic and inherited sensorineural deafness
Xavier Estivill, Paolo Fortina, Saul Surrey et al. · The Lancet · 1998 · 642 citations · Full text