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See Latest ArticlesNew mutation of the patched homologue 1 gene in a Chinese family with naevoid basal cell carcinoma syndrome
British Journal of Oral & Maxillofacial Surgery, 06/15/09
Wang W et al. - The findings suggest that the 3146A-T mutation in the PTCH gene may be the cause of NBCCS by affecting the conformation and function of the PTCH protein.
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Pediatric cholesteatoma and variants in the gene encoding connexin 26
The Laryngoscope, 11/03/09
Audit of frequent attendees to an ENT emergency clinic
The Journal of Laryngology & Otology, 11/03/09
Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations
Audiology & Neuro-Otology, 11/05/09
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