Indexed keywords
TRANSCRIPTION FACTOR;
TRANSCRIPTION FACTOR RUNX2;
UNCLASSIFIED DRUG;
ADOLESCENT;
ADULT;
AGED;
ARTICLE;
AUDIOMETRY;
AUDITORY TUBE DYSFUNCTION;
AUTOSOMAL DOMINANT DISORDER;
BONE DISEASE;
CHILD;
CLAVICLE;
CLAVICULAR APLASIA;
CLAVICULAR HYPOPLASIA;
CLEIDOCRANIAL DYSPLASIA;
CLINICAL ARTICLE;
CONDUCTION DEAFNESS;
FEMALE;
GENE EXPRESSION;
GENE MUTATION;
HEARING;
HEARING LOSS;
HIGH ARCHED PALATE;
HUMAN;
MALE;
OTITIS MEDIA;
PALATE;
PERCEPTION DEAFNESS;
PHYSICAL EXAMINATION;
PRIORITY JOURNAL;
SKULL SUTURE;
TEMPORAL BONE;
ADOLESCENT;
ADULT;
AGED;
AUDIOMETRY, PURE-TONE;
AUDITORY THRESHOLD;
BONE CONDUCTION;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME ABERRATIONS;
CHROMOSOMES, HUMAN, PAIR 6;
CLEIDOCRANIAL DYSPLASIA;
CORE BINDING FACTOR ALPHA 1 SUBUNIT;
EUSTACHIAN TUBE;
FEMALE;
GENES, DOMINANT;
HEARING LOSS, CONDUCTIVE;
HEARING LOSS, SENSORINEURAL;
HUMANS;
MALE;
MIDDLE AGED;
MUTATION;
NEOPLASM PROTEINS;
TRANSCRIPTION FACTORS;
1
0033048965
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Otto, F.1
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Crompton, T.3
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Congenital anomalies of the middle ear: Presentation of two cases
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Das gehororhan bei den angeborenen kopfmissbildungen
Nager FR, De Reynier JP. Das Gehororhan bei den Angeborenen Kopfmissbildungen. Pract Otorhinolaryngol 1948;10(Suppl 2):1.
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De Reynier, J.P.2
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Deafness and cleidocranial dysostosis
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A case of dysostosis cleido cranialis with mixed deafness
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Gay, I.1
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Congenital shoulder-neck-auditory anomalies
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Ear malformations in cleidocranial dysostosis
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Fons, M.1
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Hearing loss as a presenting symptom of cleidocranial dysplasia
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CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia
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