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Dive into the research topics of 'CDH23 mutation and phenotype heterogeneity: A profile of 107 diverse families with Usher syndrome and nonsyndromic deafness'. Together they form a unique fingerprint.- Sort by
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L. M. Astuto, J. M. Bork, M. D. Weston, J. W. Askew, R. R. Fields, D. J. Orten, S. J. Ohliger, S. Riazuddin, R. J. Morell, S. Khan, S. Riazuddin, H. Kremer, P. Van Hauwe, C. G. Moller, C. W.R.J. Cremers, C. Ayuso, J. R. Heckenlively, K. Rohrschneider, U. Spandau, J. Greenberg
Research output: Contribution to journal › Article › peer-review