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Wiley, Pediatric Dermatology, 3(29), p. 349-357

DOI: 10.1111/j.1525-1470.2011.01425.x

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Extending the Phenotypic Spectrum of Keratitis‐Ichthyosis‐Deafness Syndrome: Report of a Patient with GJB2 (G12R) Connexin 26 Mutation and Unusual Clinical Findings

Journal article published in 2011 by Tamara Lazic, Qiaoli Li ORCID, Michael Frank, Jouni Uitto, Linda H. Zhou
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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