7 results on '"Parodi, Marine"'
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2. RIPOR2: A new gene of non‐syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models.
3. Le dépistage néonatal de la surdité
4. MED12 missense mutation in a three-generation family. Clinical characterization of MED12-related disorders and literature review
5. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
6. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
7. [Neonatal hearing screening].
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