Congenital profound sensorineural deafness and oligodontia: a new syndrome.
Identifieur interne : 00E423 ( Main/Merge ); précédent : 00E422; suivant : 00E424Congenital profound sensorineural deafness and oligodontia: a new syndrome.
Auteurs : L. Glass ; R J GorlinSource :
- Archives of otolaryngology (Chicago, Ill. : 1960) [ 0003-9977 ] ; 1979.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Malformations dentaires, Surdité neurosensorielle.
- imagerie diagnostique : Denture mixte, Mâchoire partiellement édentée.
- Enfant, Femelle, Gènes récessifs, Humains, Mâle, Radiographie, Surdité neurosensorielle, Syndrome.
English descriptors
- KwdEn :
- MESH :
- congenital : Hearing Loss, Sensorineural.
- diagnostic imaging : Dentition, Mixed, Jaw, Edentulous, Partially.
- genetics : Hearing Loss, Sensorineural, Tooth Abnormalities.
- Child, Female, Genes, Recessive, Humans, Male, Radiography, Syndrome.
PubMed: 485932
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pubmed:485932Le document en format XML
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