Diagnostic genome sequencing improves diagnostic yield in a single center study of 100 patients with non-syndromic and syndromic hearing impairment.
Autor: | Dahl Rendtorff, N.1, Tranebjærg, L.1,2, Bertelsen, M.1 |
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Zdroj: | Journal of Hearing Science. Sep2024, Vol. 14 Issue 3, p122-123. 2p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |