A particular case of deafness-oligodontia syndrome

Author:

Marlin Sandrine,Denoyelle Françoise,Busquet Denise,Garabedian Noël,Petit Christine

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference30 articles.

1. Audiometric identification of normal hearing carriers of genes for deafness;Anderson;Acta. Oto-Laryngol.,1968

2. Lacrimo-auriculo-dento-digital (LADD) syndrome;Calabro;Eur. J. Pediatr.,1987

3. Congenital profound sensorineural deafness and oligodontia: a new syndrome;Glass;Arch. Otolaryngol.,1979

4. R. Gorlin, Genetic hearing loss associated with oral and dental disorders. In: R. Gorlin, H. Toriello, M. Cohen (Eds.), Hereditary Hearing Loss and its Syndromes, Oxford University Press, New York, 1995, pp. 413–417.

5. Sensorineural hearing loss, enamel hypoplasia and nail abnormalities in sibs;Heimler;Am. J. Med. Genet.,1991

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