Molecular analysis in diagnostic procedure of hearing impairment in newborns.

@article{Zaputovi2005MolecularAI,
  title={Molecular analysis in diagnostic procedure of hearing impairment in newborns.},
  author={Sanja Brajnovi{\'c} Zaputovi{\'c} and Tea {\vS}timac and Igor Prpi{\'c} and Vesna Mahulja-Stamenkovi{\'c} and Igor Medica and Borut Peterlin},
  journal={Croatian medical journal},
  year={2005},
  volume={46 5},
  pages={797-800}
}
AIM To determine the proportion of newborns diagnosed with hearing impairment through the hearing impairment screening program in newborns, and the frequency of 35delG/GJB2 mutation as a cause of hearing impairment. The results of the study imply the integration of the mutation analysis in the neonatal screening program. METHODS Evoked otoacustic emission… CONTINUE READING