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Dive into the research topics of 'Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2'. Together they form a unique fingerprint.- Sort by
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Gabriele Richard, Nkecha Brown, Akemi Ishida-Yamamoto, Alfons Krol
Research output: Contribution to journal › Article › peer-review