A comprehensive genotype-phenotype evaluation of eight Chinese probands with Waardenburg syndrome
Abstract Background Waardenburg syndrome (WS) is the most common form of syndromic deafness with phenotypic and genetic heterogeneity in the Chinese population. This study aimed to clarify the clinical characteristics and the genetic cause in eight Chinese WS families (including three familial and f...
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2022-11-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |