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Volumn 44, Issue 1, 1999, Pages 60-62

Autosomal dominant onychodystrophy and congenital sensorineural deafness

Author keywords

Autosomal dominant inheritance; Deafness; Onychodystrophy

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; FEMALE; GENE MAPPING; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; INHERITANCE; MALE; NAIL DYSTROPHY; PEDIGREE ANALYSIS; PERCEPTION DEAFNESS;

EID: 0032939395     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380050109     Document Type: Article
Times cited : (8)

References (6)
  • 1
    • 0016590597 scopus 로고
    • Congenital sensori-neural deafness associated with onycho-osteodystrophy and mental retardation (DOOR syndrome)
    • Cantwell RJ (1975) Congenital sensori-neural deafness associated with onycho-osteodystrophy and mental retardation (DOOR syndrome). Humangenetik 26: 261-265
    • (1975) Humangenetik , vol.26 , pp. 261-265
    • Cantwell, R.J.1
  • 3
    • 0027443757 scopus 로고
    • DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): A new patient and delineation of neurologic variability among recessive cases
    • Lin HJ, Kakkis ED, Eteson DJ, Lachman RS (1993) DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): A new patient and delineation of neurologic variability among recessive cases. Am J Med Genet 47: 534-539
    • (1993) Am J Med Genet , vol.47 , pp. 534-539
    • Lin, H.J.1    Kakkis, E.D.2    Eteson, D.J.3    Lachman, R.S.4
  • 5
    • 0344365644 scopus 로고
    • Familial ectodermal dysplasia with sensori-neural deafness and other anomalies
    • Robinson GC, Miller JR, Bensimon JR (1962) Familial ectodermal dysplasia with sensori-neural deafness and other anomalies. Pediatrics 30: 797-802
    • (1962) Pediatrics , vol.30 , pp. 797-802
    • Robinson, G.C.1    Miller, J.R.2    Bensimon, J.R.3
  • 6
    • 0019858720 scopus 로고
    • The deafness, onycho-osteodystrophy, mental retardation syndrome
    • Sanchez O, Mazas JJM, de Dematos IO (1981) The deafness, onycho-osteodystrophy, mental retardation syndrome. Hum Genet 58: 228-230
    • (1981) Hum Genet , vol.58 , pp. 228-230
    • Sanchez, O.1    Mazas, J.J.M.2    De Dematos, I.O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.