A comparative study of hearing loss in two microdeletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) Syndromes

Journal of Pediatrics

Volumn 158, Issue 2, 2011, Pages 301-306

  Zarchi, Omer ^a,b,e   Attias, Josef ^b,c   Raveh, Eyal ^b,f   Basel Vanagaite, Lina ^d,f   Saporta, Liron ^a,e   Gothelf, Doron ^a,f  

^a SHEBA MEDICAL CENTER   (Israel)

^b SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL   (Israel)

^c UNIVERSITY OF HAIFA   (Israel)

^d RABIN MEDICAL CENTER   (Israel)

^e Interdisciplinary PhD Program in Neuroscience Tel Aviv   (Israel)

^f TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

CATECHOL METHYLTRANSFERASE;

ACOUSTIC REFLEX; ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHROMOSOME ABERRATION; CHROMOSOME DELETION 22Q11; COMPARATIVE STUDY; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; DNA POLYMORPHISM; FEMALE; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; MIXED HEARING LOSS; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; VELOCARDIOFACIAL SYNDROME; WILLIAM SYNDROME;

ANALYSIS OF VARIANCE; AUDIOMETRY, PURE-TONE; AUDITORY THRESHOLD; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 7; DIGEORGE SYNDROME; FEMALE; FOLLOW-UP STUDIES; HEARING LOSS; HEARING LOSS, CONDUCTIVE; HEARING LOSS, SENSORINEURAL; HUMANS; INCIDENCE; INFANT; MALE; SEVERITY OF ILLNESS INDEX; WILLIAMS SYNDROME;

EID: 78651488695     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2010.07.056     Document Type: Article

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