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Volumn 5, Issue 4, 1996, Pages 543-547

The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANADA; CENTROMERE; CHROMOSOME 13Q; CLINICAL ARTICLE; ECTODERMAL DYSPLASIA; GENE MAPPING; GENETIC LINKAGE; HAIR DISEASE; HAPLOTYPE; HUMAN; HUMAN CELL; KERATOSIS PALMOPLANTARIS; NAIL DYSTROPHY; PRIORITY JOURNAL; TELOMERE;

EID: 0029881589     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.4.543     Document Type: Article
Times cited : (54)

References (34)
  • 1
    • 0014194680 scopus 로고
    • Hydrotic ectodermal dysplasia-Clouston's family revisited
    • Williams, M. and Fraser, F C. (1967) Hydrotic ectodermal dysplasia-Clouston's family revisited. Can. Med. Ass. J., 96, 36-38.
    • (1967) Can. Med. Ass. J. , vol.96 , pp. 36-38
    • Williams, M.1    Fraser, F.C.2
  • 2
    • 0021333491 scopus 로고
    • Oral findings of Clouston's syndrome (hidrotic ectodermal dysplasia)
    • George, D.I. and Escobar, V H. (1984) Oral findings of Clouston's syndrome (hidrotic ectodermal dysplasia). Oral Surg., 57, 258-262.
    • (1984) Oral Surg. , vol.57 , pp. 258-262
    • George, D.I.1    Escobar, V.H.2
  • 3
    • 0002760563 scopus 로고
    • Hereditary ectodermal dystrophy
    • Clouston, H.R. (1929) Hereditary ectodermal dystrophy Can. Med. Ass. J., 21, 18-31.
    • (1929) Can. Med. Ass. J. , vol.21 , pp. 18-31
    • Clouston, H.R.1
  • 5
    • 0017334372 scopus 로고
    • Hidrotic ectodermal dysplasia
    • Rajagopalan, K. and Hai Tai, C (1977) Hidrotic ectodermal dysplasia. Arch. Dermatol., 113, 481-485
    • (1977) Arch. Dermatol. , vol.113 , pp. 481-485
    • Rajagopalan, K.1    Hai Tai, C.2
  • 7
    • 0025766267 scopus 로고
    • Clouston syndrome: A rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia
    • Patel, R.A, Bixler, D. and Norins A.L (1991) Clouston syndrome: a rare autosomal dominant trait with palmoplantar hyperkeratosis and alopecia. J. Craniofac. Gen. Dev. Biol., 11, 176-179.
    • (1991) J. Craniofac. Gen. Dev. Biol. , vol.11 , pp. 176-179
    • Patel, R.A.1    Bixler, D.2    Norins, A.L.3
  • 8
    • 0017132801 scopus 로고
    • Hidrotic ectodermal dysplasia in a black mother and daughter
    • Mcnaughton, P.Z., Pierson, L. and Rodman, G. (1976) Hidrotic ectodermal dysplasia in a black mother and daughter. Arch. Dermatol., 112, 1448-1450.
    • (1976) Arch. Dermatol. , vol.112 , pp. 1448-1450
    • Mcnaughton, P.Z.1    Pierson, L.2    Rodman, G.3
  • 11
    • 0015400958 scopus 로고
    • Properties of hair keratin in an autosomal dominant form of ectodermal dysplasia
    • Gold, R.J.M. and Scriver, C.R. (1972) Properties of hair keratin in an autosomal dominant form of ectodermal dysplasia. Am. J. Hum. Genet., 24, 549-561.
    • (1972) Am. J. Hum. Genet. , vol.24 , pp. 549-561
    • Gold, R.J.M.1    Scriver, C.R.2
  • 13
    • 0027480639 scopus 로고
    • A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex
    • Hovnanian, A., Pollack, E., Hilal, L., Rochat, A., Prost, C., Barrandon, Y. and Goossens, M. (1993) A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex. Nature Genet. 3, 327-332.
    • (1993) Nature Genet. , vol.3 , pp. 327-332
    • Hovnanian, A.1    Pollack, E.2    Hilal, L.3    Rochat, A.4    Prost, C.5    Barrandon, Y.6    Goossens, M.7
  • 16
    • 0028279523 scopus 로고
    • Epidermal disease: Faulty keratin filaments take their toll
    • Compton, J G. (1994) Epidermal disease: faulty keratin filaments take their toll. Nature Genet. 6, 6-7.
    • (1994) Nature Genet. , vol.6 , pp. 6-7
    • Compton, J.G.1
  • 18
    • 0023867610 scopus 로고
    • A group of type I keratin genes on human chromosome 17: Characterization and expression
    • Rosenberg, M., RayChaudhury, A., Shows, T B., Le Beau, M.M. and Fuchs, E. (1988) A group of type I keratin genes on human chromosome 17: characterization and expression Mol. Cell Biol. 8, 722-736.
    • (1988) Mol. Cell Biol. , vol.8 , pp. 722-736
    • Rosenberg, M.1    RayChaudhury, A.2    Shows, T.B.3    Le Beau, M.M.4    Fuchs, E.5
  • 19
    • 0027323058 scopus 로고
    • Organization and expression of hair follicles
    • Rogers, G.E. and Powell. B.C. (1993) Organization and expression of hair follicles. J. Invest. Dermatol 101, 50S-55S.
    • (1993) J. Invest. Dermatol , vol.101
    • Rogers, G.E.1    Powell, B.C.2
  • 26
    • 0029149080 scopus 로고
    • A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsydromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)
    • Guilford, P., Dodé, C., Crozet F., Blanchard, S., Chaib, H., Levilliers, J., LeviAcobas, F., Weil, D., Weissenbach, J., Cohen, D., Le Paslier, D., Kaplan, J-C. and Petit, C. (1995) A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsydromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C). Genomics 29, 163-169.
    • (1995) Genomics , vol.29 , pp. 163-169
    • Guilford, P.1    Dodé, C.2    Crozet, F.3    Blanchard, S.4    Chaib, H.5    Levilliers, J.6    Leviacobas, F.7    Weil, D.8    Weissenbach, J.9    Cohen, D.10    Le Paslier, D.11    Kaplan, J.-C.12    Petit, C.13
  • 28
    • 0024150761 scopus 로고
    • Structural abnormalities of the epidermally derived appendages in skin from patients with ectodermal dysplasia: Insights into developmental errors
    • Holbrook, K.A. (1988) Structural abnormalities of the epidermally derived appendages in skin from patients with ectodermal dysplasia: insights into developmental errors. Birth Defects Original Article Series. 24, 15-44.
    • (1988) Birth Defects Original Article Series , vol.24 , pp. 15-44
    • Holbrook, K.A.1
  • 29
  • 30
    • 0028555358 scopus 로고
    • A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval
    • Chaib, H., Lina-Granade, G., Guilford, P., Plauchu, H., Levilliers, J., Morgon, A. and Petit, C. (1994) A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum. Mol. Genet. 3, 2219-2222
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 2219-2222
    • Chaib, H.1    Lina-Granade, G.2    Guilford, P.3    Plauchu, H.4    Levilliers, J.5    Morgon, A.6    Petit, C.7
  • 34
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop, G.M., Lalouel, J.M., Julier, C. and Ott, J (1985) Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am. J. Hum. Genet 37, 482-498.
    • (1985) Am. J. Hum. Genet , vol.37 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.