Universal Screening for Congenital Hearing Loss

This publication has 15 references indexed in Scilit:

• Genetic causes of nonsyndromic hearing loss
  Current Opinion in Pediatrics, 1999
• Confirmation of deafness in infancy
  Archives of Disease in Childhood, 1999
• Carrier Rates in the Midwestern United States for GJB2 Mutations Causing Inherited Deafness
  JAMA, 1999
• Age at Implantation: Its Importance in Pediatric Cochlear Implantation
  The Laryngoscope, 1999
• THE CASE FOR EARLY IDENTIFICATION OF HEARING LOSS IN CHILDREN
  Pediatric Clinics of North America, 1999
• The Newborn With Hearing Loss: Detection in the Nursery
  Pediatrics, 1998
• The Rhode Island Hearing Assessment Program: Experience with statewide hearing screening (1993-1996)
  The Journal of Pediatrics, 1998
• Connexin-26 mutations in sporadic and inherited sensorineural deafness
  The Lancet, 1998
• Effect of altered neuronal activity on cell size in the medial nucleus of the trapezoid body and ventral cochlear nucleus of the gerbil
  Journal of Comparative Neurology, 1994
• Conductive Hearing Loss During Infancy
  Journal of Speech, Language, and Hearing Research, 1991