Auditory pathology in cri-du-chat (5p-) syndrome: Phenotypic evidence for auditory neuropathy

Clinical Genetics

Volumn 72, Issue 4, 2007, Pages 369-373

  Swanepoel, Dewet ^a  

^a UNIVERSITY OF PRETORIA   (South Africa)

Author keywords

5p deletion; Auditory brainstemr response; Auditory neuropathy; B catenin; Cochlear microphonic; Cri du chat syndrome; Hearing loss

Indexed keywords

BETA CATENIN;

ARTICLE; CASE REPORT; CAT CRY SYNDROME; CHROMOSOME 5P; CHROMOSOME DELETION; CHROMOSOME MAP; CLINICAL FEATURE; COCHLEA POTENTIAL; DISEASE SEVERITY; EVOKED AUDITORY RESPONSE; FEMALE; HEARING LOSS; HUMAN; KARYOTYPE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN EXPRESSION; SOUND LEVEL MEASUREMENT; VESTIBULOCOCHLEAR NERVE DISEASE;

BETA CATENIN; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 5; CRI-DU-CHAT SYNDROME; CYTOGENETICS; ELECTROPHYSIOLOGY; FEMALE; GENOTYPE; HEARING LOSS; HUMANS; INFANT; KARYOTYPING; NERVOUS SYSTEM DISEASES; PHENOTYPE; SYNDROME;

EID: 34548548469     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2007.00870.x     Document Type: Article

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