General ENT News

ENT

sponsor
Become a Member Today!
Register
Email:


Password:

Remember me
Forgot your Password?
Invite Code?
Article ID

Your Article Summary

(Click the title below to leave the MDLinx Network and go to the Journal's Website)

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.


Today in Basic Science/Genetics...keeping you current

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

Article Search

Keyword:

Search:

Published within

Sort By:
Date
Relevance


Sponsor

Send this Summary to a Colleague

Enter email address