Hereditary Hearing Loss
Publisher
Springer New York
Reference42 articles.
1. Abdelhak, S., Kalatzis, V., Heilig, R., et al. (1997). A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome gene and identifies a novel gene family. Nature Genetics, 15, 157–164. 2. Abe, S., Usami, S., Shinkawa, H., et al. (2000). Prevalent connexin 26 gene (GJB2) mutations in Japanese. Journal of Medical Genetics, 37, 41–43. 3. ACMG Statement. (2002). Genetics evaluation guidelines for the etiologic diagnosis of congenital hearing loss. Genetic evaluation of congenital hearing loss expert panel ACMG statement. Genetics in Medicine, 4, 162–171. 4. Azaiez, H., Booth, K. T., Bu, F., et al. (2014). TBC1D24 mutation causes autosomal dominant non-syndromic hearing loss. Human Mutation, 35, 819–823. 5. Bachmann, K. R., & Arvedson, J. C. (1998). Early identification and intervention for children who are hearing impaired. Pediatrics in Review, 19, 155–164.
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