Ear and hearing problems in relation to karyotype in children with Turner syndrome

Hearing Research

Volumn 275, Issue 1-2, 2011, Pages 81-88

  Verver, E J J ^a   Freriks, K ^a   Thomeer, H G X M ^a   Huygen, P L M ^a   Pennings, R J E ^a   Alfen van der Velden, A A E M ^a   Timmers, H J ^a   Otten, B J ^a   Cremers, C W R J ^a   Kunst, H P M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUDITORY THRESHOLD; CHILD; CHROMOSOME DELETION; CLINICAL ARTICLE; CONTROLLED STUDY; EARDRUM; FEMALE; HEARING DISORDER; HUMAN; ISOCHROMOSOME; KARYOTYPE; MIDDLE EAR; MONOSOMY; MOSAICISM; OTITIS MEDIA; PRESCHOOL CHILD; PREVALENCE; PRIORITY JOURNAL; RECURRENT DISEASE; RETROSPECTIVE STUDY; SCHOOL CHILD; TURNER SYNDROME; X CHROMOSOME;

ADOLESCENT; ADULT; AUDIOLOGY; AUDIOMETRY; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, X; EAR DISEASES; FEMALE; GENE DELETION; HEARING; HEARING DISORDERS; HUMANS; INFANT; ISOCHROMOSOMES; KARYOTYPING; MALE; MOSAICISM; TURNER SYNDROME;

EID: 79955978421     PISSN: 03785955     EISSN: 18785891     Source Type: Journal    
DOI: 10.1016/j.heares.2010.12.007     Document Type: Article

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