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European Journal of Endocrinology
Volumn 135, Issue 4, 1996, Pages 394-395
Thyroid disease and hearing disorders: New genetic links
Author keywords

[No Author keywords available]
Indexed keywords

CHROMOSOME 7Q; DISEASE ASSOCIATION; GENETIC LINKAGE; HEARING DISORDER; HUMAN; PENDRED SYNDROME; PRIORITY JOURNAL; SHORT SURVEY; THYROID DISEASE;
EID: 0029856879     PISSN: 08044643     EISSN: None     Source Type: Journal    
DOI: 10.1530/eje.0.1350394     Document Type: Short Survey
Times cited : (3)
References (6)
  • 1
    • 0028107231 scopus 로고
    • Alpha and beta thyroid hormone receptor (TR) gene expression during auditory neurogenesis: Evidence for TR isoform-specific transcriptional regulation in vivo
    • Bradley DJ, Towle HC, Young WS. Alpha and beta thyroid hormone receptor (TR) gene expression during auditory neurogenesis: evidence for TR isoform-specific transcriptional regulation in vivo. Proc Natl Acad Sci USA 1994;91:439-43
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 439-443
    • Bradley, D.J.1    Towle, H.C.2    Young, W.S.3
  • 2
    • 0028882610 scopus 로고
    • Genetic and clinical features of 42 kindreds with resistance to thyroid hormone
    • Brucker-Davis F, Skarulis MC, Grace MB, et al. Genetic and clinical features of 42 kindreds with resistance to thyroid hormone. Ann Int Med 1995;123:572-83
    • (1995) Ann Int Med , vol.123 , pp. 572-583
    • Brucker-Davis, F.1    Skarulis, M.C.2    Grace, M.B.3
  • 4
    • 0346154518 scopus 로고
    • Association of congenital deafness with goiter (Pendred's syndrome); a study of 207 families
    • Fraser GR. Association of congenital deafness with goiter (Pendred's syndrome); a study of 207 families. Ann Hum Genet 1965;28:201-49
    • (1965) Ann Hum Genet , vol.28 , pp. 201-249
    • Fraser, G.R.1
  • 5
    • 8244263673 scopus 로고    scopus 로고
    • Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the syndromic deafness gene DFNB4
    • Coyle B, Coffey R, Armour JAL, et al. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the syndromic deafness gene DFNB4. Nature Genet 1996;12:421-3
    • (1996) Nature Genet , vol.12 , pp. 421-423
    • Coyle, B.1    Coffey, R.2    Armour, J.A.L.3
  • 6
    • 0029963073 scopus 로고    scopus 로고
    • Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification
    • Sheffield VC, Kraiem Z, Beck JC, et al. Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification. Nature Genet 1996;12:424-6
    • (1996) Nature Genet , vol.12 , pp. 424-426
    • Sheffield, V.C.1    Kraiem, Z.2    Beck, J.C.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.