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See Latest ArticlesThe 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3
Journal of Cranio-Maxillofacial Surgery, 06/17/09
Dostal A et al. - Orofacial abnormalities are characteristic features of 18q- syndrome patients and potential CP/L critical region could be assumed at 18q22.3 between markers D18S879 and D18S1141. In addition, gene deficient mouse models for Sall3 or Tshz1 genes, which are located at the 18q22.3 critical region, displayed palate abnormality phenotype.
Today in Basic Science/Genetics...keeping you current
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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
Today in Oral Cavity...keeping you current
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Update on oral lichen planus
Expert Review of Dermatology, 10/14/09
Oral Allergy Syndrome
Allergology International, 10/30/09
Conducting oral examinations for cancer in general practice: what are the barriers?
Family Practice, 10/16/09
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