| http://www.w3.org/ns/prov#value | - The evaluation, therefore, should include a review of family history of specific genetic disorders or syndromes, including genetic testing for gene mutations such as GJB2 (connexin-26), and syndromes commonly associated with early-onset childhood sensorineural hearing loss (Appendix 1; Denoyelle et al., 1999; Nance, 2003; Nance & Kearsey, 2004; Santos et al., 2005).
|
