- Keratitis - ichthyosis - deafness syndrome: connexin 26 (GJB2) mutati…
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Keratitis - ichthyosis - deafness syndrome: connexin 26 (GJB2) mutations in two patients

  1. HOLOBRADÁ, Mariana et al. Keratitis - ichthyosis - deafness syndrome: connexin 26 (GJB2) mutations in two patients. In Česko-slovenská dermatologie. ISSN 0009-0514. Praha : Česká lékařská společnost J. Ev. Purkyně, 2010, 2010, roč. 85, č. 4, s. 240.
Number of the records: 1  

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