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Volumn 106, Issue 8, 1996, Pages 992-997

Hearing loss in Turner syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; HEARING LOSS; HUMAN; MALE; MEDICAL CARE; MEDICAL RECORD; OTITIS MEDIA; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; QUESTIONNAIRE; RETROSPECTIVE STUDY; RIEGER SYNDROME; SCHOOL CHILD; SHORT STATURE; TURNER SYNDROME; X CHROMOSOME ABERRATION;

EID: 0029827734     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-199608000-00015     Document Type: Article
Times cited : (45)

References (11)
  • 1
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    • Tesch LG, Rodriguez-Rigau LJ, et al. Recommendations for diagnosis, treatment and management of individuals with Turner syndrome.
    • Rosenfield RG, Tesch LG, Rodriguez-Rigau LJ, et al. Recommendations for diagnosis, treatment and management of individuals with Turner syndrome. Endocrinologist. 1994;4: 351-358.
    • Endocrinologist. 1994;4: 351-358.
    • Rosenfield, R.G.1
  • 4
  • 5
    • 0028291185 scopus 로고    scopus 로고
    • Sylven L, Borg E. Ear and hearing problems in 44 middle-aged women with Turner's syndrome.
    • Hultzcranz M, Sylven L, Borg E. Ear and hearing problems in 44 middle-aged women with Turner's syndrome. Hear Res. 1994;76:127-132.
    • Hear Res. 1994;76:127-132.
    • Hultzcranz, M.1
  • 6
    • 0025763762 scopus 로고    scopus 로고
    • Stekal L, Schatz D, et al. The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype.
    • Mathur A, Stekal L, Schatz D, et al. The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype. Am J Hum Genet. 1991;48:682-686.
    • Am J Hum Genet. 1991;48:682-686.
    • Mathur, A.1
  • 7
    • 0027526217 scopus 로고    scopus 로고
    • Skoletsky J, Shuber AP, et al. Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs.
    • Richards B, Skoletsky J, Shuber AP, et al. Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs. Hum Mol Genet. 1992;2:159-163.
    • Hum Mol Genet. 1992;2:159-163.
    • Richards, B.1
  • 8
    • 0026678490 scopus 로고    scopus 로고
    • Zoghbi HY, Mosely AB, et al. Methylation of Hpall and Hhal sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.
    • Alien RC, Zoghbi HY, Mosely AB, et al. Methylation of Hpall and Hhal sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. AmJHumGenet. 1992;51:1229-1239.
    • AmJHumGenet. 1992;51:1229-1239.
    • Alien, R.C.1
  • 9
    • 0025371201 scopus 로고    scopus 로고
    • Kwitek AE, May PE, et al. Dinucleotide repeat polymorphism at the DXS453, DXS454, and DXS458 loci.
    • Weber JL, Kwitek AE, May PE, et al. Dinucleotide repeat polymorphism at the DXS453, DXS454, and DXS458 loci. Nucleic Acids Res. 1990;18:4037.
    • Nucleic Acids Res. 1990;18:4037.
    • Weber, J.L.1
  • 10
    • 0025943652 scopus 로고    scopus 로고
    • Fenwick G, Chamberlain JS, et al. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphism.
    • Clemens PR, Fenwick G, Chamberlain JS, et al. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphism. Am JHum Genet. 1991;49:951-960.
    • Am JHum Genet. 1991;49:951-960.
    • Clemens, P.R.1
  • 11
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    • Booms PFM, Vossen RHAM, CA. Repeat polymorphism near DXS418 (P122).
    • Van de Vosses E, Booms PFM, Vossen RHAM, CA. Repeat polymorphism near DXS418 (P122). Hum Mol Genet. 1993;2: 2202.
    • Hum Mol Genet. 1993;2: 2202.
    • Van De Vosses, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.