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Volumn 71, Issue 1, 2007, Pages 169-174

Novel EYA1 mutation in a Korean branchio-oto-renal syndrome family

Author keywords

BOR; Branchio oto renal syndrome; EYA1; Korean; Mutation

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRANCHIOGENIC CYST; BRANCHIOOTORENAL SYNDROME; CHROMOSOME 8Q; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSTIC IMAGING; DNA SEQUENCE; EVOKED BRAIN STEM AUDITORY RESPONSE; EXON; EXTERNAL EAR MALFORMATION; EYA1 GENE; FEMALE; GENE; HUMAN; IMAGE ANALYSIS; MALE; MICROTIA; MIDDLE EAR MALFORMATION; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; SECRETORY OTITIS MEDIA; SEQUENCE ANALYSIS; SOUTH KOREA; SYMPTOM; TYMPANOMETRY;

EID: 33845620343     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijporl.2006.08.023     Document Type: Article
Times cited : (14)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.