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Dive into the research topics of 'Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome'. Together they form a unique fingerprint.- Sort by
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M. Andrew Nesbit, Michael R. Bowl, Brian Harding, Asif Ali, Alejandro Ayala, Carol Crowe, Angus Dobbie, Geeta Hampson, Ian Holdaway, Michael A. Levine, Robert McWilliams, Susan Rigden, Julian Sampson, Andrew J. Williams, Rajesh V. Thakker
Research output: Contribution to journal › Article › peer-review