DOI: 10.1055/s-00000067

Seminars in Hearing

References

Cohn ES, Kelley PM.
Clinical phenotype and mutations in Connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss 
Am J Med Genet 1999; 89: 130-136  

Download Bibliographical Data

Search in:
Access:
Access: