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Volumn 126, Issue 9, 2000, Pages 1065-1069

Sensorineural hearing loss and Mondini dysplasia caused by a deletion at locus DFN3

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUDIOMETRY; CASE REPORT; CHILD; CHROMOSOME DELETION X; CLINICAL ARTICLE; DNA SEQUENCE; FEMALE; GENE LOCUS; GENOTYPE; HEARING LOSS; HUMAN; MALE; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS;

EID: 0033821529     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.126.9.1065     Document Type: Article
Times cited : (33)

References (24)
  • 1
    • 0007992841 scopus 로고
    • Grupo multicentrico de deteccion precoz de la sordera. Deteccion precoz de la hipoacusia infantil en recien nacidos de alto riesgo: Estudio multicentrico
    • (1994) An Esp Pediatr , pp. 15-20
  • 11
    • 8244263673 scopus 로고    scopus 로고
    • Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsydromic deafness gene DFNB4
    • (1996) Nat Genet , vol.12 , pp. 421-423
    • Coyle, B.1    Coffey, R.2    Armour, J.A.L.3
  • 19
    • 0001775875 scopus 로고    scopus 로고
    • The X-linked recessive progressive mixed hearing loss syndrome with perilymphatic gusher during stapes surgery (DFN3)
    • Martini A, Read A, Stephens D, eds. Genetics and Hearing Impairment. London, England: Whurr Publishers
    • (1996) , pp. 236-243
    • Cremers, C.R.W.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.