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Volumn 27, Issue 2, 1998, Pages 121-124
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Otodental syndrome
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Author keywords
Ectodermal dysplasia; Otodental syndrome; Sensorineural hearing loss
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Indexed keywords
ARTICLE;
CASE REPORT;
CHILD;
CONGENITAL MALFORMATION;
DOMINANT GENE;
ECTODERMAL DYSPLASIA;
GENETICS;
HUMAN;
MALE;
MOLAR TOOTH;
PATHOLOGY;
PERCEPTION DEAFNESS;
SYNDROME;
TOOTH CROWN;
TOOTH MALFORMATION;
CHILD;
ECTODERMAL DYSPLASIA;
GENES, DOMINANT;
HEARING LOSS, SENSORINEURAL;
HUMANS;
MALE;
MOLAR;
SYNDROME;
TOOTH ABNORMALITIES;
TOOTH CROWN;
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EID: 0032043643
PISSN: 09015027
EISSN: None
Source Type: Journal
DOI: 10.1016/S0901-5027(98)80309-3 Document Type: Article |
Times cited : (21)
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References (17)
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