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Volumn 60, Issue 4, 1998, Pages 224-226

Late-onset sensorineural hearing loss in Coffin-Lowry syndrome

Author keywords

Coffin Lowry syndrome; Sensorineural hearing loss

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL BONE DISEASE; FACIES; HEARING AID; HUMAN; MALE; MENTAL DEFICIENCY; ONSET AGE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0031813063     PISSN: 03011569     EISSN: None     Source Type: Journal    
DOI: 10.1159/000027598     Document Type: Article
Times cited : (7)

References (14)
  • 1
    • 0000979928 scopus 로고
    • Mental retardation with osteocartilaginous anomalies
    • Coffin GS, Siris E, Wegienka LC: Mental retardation with osteocartilaginous anomalies. Am J Dis Child 1966,112:205-213.
    • (1966) Am J Dis Child , vol.112 , pp. 205-213
    • Coffin, G.S.1    Siris, E.2    Wegienka, L.C.3
  • 2
    • 0015073716 scopus 로고
    • A new dominant gene mental retardation syndrome
    • Lowry B, Miller JR, Fraser FC: A new dominant gene mental retardation syndrome. Am J Dis Child 1971;121:491-500.
    • (1971) Am J Dis Child , vol.121 , pp. 491-500
    • Lowry, B.1    Miller, J.R.2    Fraser, F.C.3
  • 3
    • 0023945707 scopus 로고
    • The Coffin-Lowry syndrome
    • Young ID: The Coffin-Lowry syndrome. J Med Genet 1988;25:344-348.
    • (1988) J Med Genet , vol.25 , pp. 344-348
    • Young, I.D.1
  • 4
    • 0020079421 scopus 로고
    • The Coffin-Lowry syndrome: Experience from four centres
    • Hunter AGW, Partington MW, Evans JA: The Coffin-Lowry syndrome: Experience from four centres. Clin Genet 1982;21:321-335.
    • (1982) Clin Genet , vol.21 , pp. 321-335
    • Hunter, A.G.W.1    Partington, M.W.2    Evans, J.A.3
  • 5
    • 0015384319 scopus 로고
    • Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's syndrome
    • Procopis PG, Turner B: Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's syndrome. Am J Dis Child 1972;124:258-261.
    • (1972) Am J Dis Child , vol.124 , pp. 258-261
    • Procopis, P.G.1    Turner, B.2
  • 6
    • 0028068827 scopus 로고
    • Construction of a high-resolution linkage map for Xp22.I-p22.2 and refinement of the genetic localisation of the Coffin-Lowry syndrome gene
    • Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PS, O'Riordan JL, Partington MW: Construction of a high-resolution linkage map for Xp22.I-p22.2 and refinement of the genetic localisation of the Coffin-Lowry syndrome gene. Genomics 1994:22:617-625.
    • (1994) Genomics , vol.22 , pp. 617-625
    • Biancalana, V.1    Trivier, E.2    Weber, C.3    Weissenbach, J.4    Rowe, P.S.5    O'Riordan, J.L.6    Partington, M.W.7
  • 8
    • 0016812249 scopus 로고
    • The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome
    • Tentamy SA, Miller JD, Hussels-Maumenee I: The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome. J Pediatr 1985;86:724-731.
    • (1985) J Pediatr , vol.86 , pp. 724-731
    • Tentamy, S.A.1    Miller, J.D.2    Hussels-Maumenee, I.3
  • 10
    • 0027475725 scopus 로고
    • Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations
    • Hartsfield JK, Hall BD, Grix AW, Koussef BG, Salazar JF, Haufe SMW: Pleiotropy in Coffin-Lowry syndrome: Sensorineural hearing deficit and premature tooth loss as early manifestations. Am J Med Genet 1993;45:552-557.
    • (1993) Am J Med Genet , vol.45 , pp. 552-557
    • Hartsfield, J.K.1    Hall, B.D.2    Grix, A.W.3    Koussef, B.G.4    Salazar, J.F.5    Haufe, S.M.W.6
  • 11
    • 0028348804 scopus 로고
    • Coffin-Lowry syndrome with sensorineural deafness and labyrinthine anomaly
    • Higashi K, Matsuki C: Coffin-Lowry syndrome with sensorineural deafness and labyrinthine anomaly. J Laryngol Otol 1994;108:147-148.
    • (1994) J Laryngol Otol , vol.108 , pp. 147-148
    • Higashi, K.1    Matsuki, C.2
  • 13
    • 0019456679 scopus 로고
    • Early recognition of the Coffin-Lowry syndrome
    • Wilson WG, Kelly TE: Early recognition of the Coffin-Lowry syndrome. Am J Med Genet 1981;8:215-220.
    • (1981) Am J Med Genet , vol.8 , pp. 215-220
    • Wilson, W.G.1    Kelly, T.E.2
  • 14


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.