K. Lewis

Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss

E. Rappaport, P. Fortina, A. Ferraris, 2002, Clinical genetics.

Parental narratives of genetic testing for hearing loss: audiologic implications for clinical work with children and families.

I. Krantz, A. Steinberg, Girija Kaimal, 2007, American journal of audiology.

Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic

I. Krantz, C. Stolle, Dinah Yaeger, 2006, American journal of medical genetics. Part A.