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NARA Subscribed2
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Springer Nature2
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Journal of Molecular Medicine2
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20071
20051
R. Caylan results 2 · Newest (Page 1/1, per page 25)
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A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2–q13.4NARA Subscribed
Journal of Molecular Medicine · 2007 · Vol. 85 · Issue 4 · Springer
E. Kalay; R. Caylan; A. F. Kıroglu; T. Yasar; R. W. J. Collin; J. G. A. M. Heister; J. Oostrik; C. W. R. J. Cremers; H. G. Brunner; A. Karaguzel; H. Kremer
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A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndromeNARA Subscribed
Journal of Molecular Medicine · 2005 · Vol. 83 · Issue 12 · Springer
E. Kalay; A. P. M. de Brouwer; R. Caylan; S. B. Nabuurs; B. Wollnik; A. Karaguzel; J. G. A. M. Heister; H. Erdol; F. P. M. Cremers; C. W. R. J. Cremers; H. G. Brunner; H. Kremer
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