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Volumn 67, Issue 2, 2000, Pages 232-236

A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11

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Indexed keywords

CONNEXIN 26;

EID: 0034661335     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6202     Document Type: Article
Times cited : (5)

References (18)
  • 2
    • 0002921779 scopus 로고
    • The major forms of hereditary ectodermal dysplasia
    • Clouston H. R. The major forms of hereditary ectodermal dysplasia. Can. Med. Assoc. J. 40:1939;1-7.
    • (1939) Can. Med. Assoc. J. , vol.40 , pp. 1-7
    • Clouston, H.R.1
  • 4
    • 0029149080 scopus 로고
    • A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory non-syndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)
    • Guilford L., Dodé C., Crozet F., Blanchard S., Chaib H., Levilliers J., Levi-Acobas F., Weil D., Weissenbach J., Cohen D., Le Paslier D., Kaplan J. C., Petit C. A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory non-syndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C). Genomics. 29:1995;163-169.
    • (1995) Genomics , vol.29 , pp. 163-169
    • Guilford, L.1    Dodé, C.2    Crozet, F.3    Blanchard, S.4    Chaib, H.5    Levilliers, J.6    Levi-Acobas, F.7    Weil, D.8    Weissenbach, J.9    Cohen, D.10    Le Paslier, D.11    Kaplan, J.C.12    Petit, C.13
  • 6
    • 0029881589 scopus 로고    scopus 로고
    • The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q
    • Kibar Z., Der Kaloustian V. M., Brais B., Hani V., Clarke Fraser F., Rouleau G. A. The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q. Hum. Mol. Genet. 5:1996;543-547.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 543-547
    • Kibar, Z.1    Der Kaloustian, V.M.2    Brais, B.3    Hani, V.4    Clarke Fraser, F.5    Rouleau, G.A.6
  • 7
    • 0033557443 scopus 로고    scopus 로고
    • A radiation hybrid map of 48 loci including the Clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q
    • Kibar Z., Lafrenière R. G., Chakravarti A., Wang J. C., Chevrette M., Der Kaloustian V. M., Rouleau G. A. A radiation hybrid map of 48 loci including the Clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q. Genomics. 56:1999;127-130.
    • (1999) Genomics , vol.56 , pp. 127-130
    • Kibar, Z.1    Lafrenière, R.G.2    Chakravarti, A.3    Wang, J.C.4    Chevrette, M.5    Der Kaloustian, V.M.6    Rouleau, G.A.7
  • 10
    • 0033563149 scopus 로고    scopus 로고
    • Cloning and characterization of RNF6, a novel RING finger gene mapping to 13q12
    • Macdonald D. H. C., Lahiri D., Sampath A., Chase A., Sohal J., Cross N. C. P. Cloning and characterization of RNF6, a novel RING finger gene mapping to 13q12. Genomics. 58:1999;94-97.
    • (1999) Genomics , vol.58 , pp. 94-97
    • Macdonald, D.H.C.1    Lahiri, D.2    Sampath, A.3    Chase, A.4    Sohal, J.5    Cross, N.C.P.6
  • 12
    • 0030911627 scopus 로고    scopus 로고
    • The gene for autosomal dominant hydrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
    • Radhakrishna U., Blouin J. L., Mehenni H., Mehta T. Y., Sheth F. J., Sheth J. J., Solanki J. V., Antonorakis S. E. The gene for autosomal dominant hydrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region. Am. J. Med. Genet. 71:1997;80-86.
    • (1997) Am. J. Med. Genet. , vol.71 , pp. 80-86
    • Radhakrishna, U.1    Blouin, J.L.2    Mehenni, H.3    Mehta, T.Y.4    Sheth, F.J.5    Sheth, J.J.6    Solanki, J.V.7    Antonorakis, S.E.8
  • 15
    • 0031860399 scopus 로고    scopus 로고
    • Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutations
    • Taylor T. D., Hayflick S. J., McKinnon W., Guttmacher A. E., Hovnanian A., Litt M., Zonana J. Confirmation of linkage of Clouston syndrome (hidrotic ectodermal dysplasia) to 13q11-q12.1 with evidence for multiple independent mutations. J. Invest. Dermatol. 111:1998;83-85.
    • (1998) J. Invest. Dermatol. , vol.111 , pp. 83-85
    • Taylor, T.D.1    Hayflick, S.J.2    McKinnon, W.3    Guttmacher, A.E.4    Hovnanian, A.5    Litt, M.6    Zonana, J.7
  • 18
    • 0030916729 scopus 로고    scopus 로고
    • Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex
    • Zhang Y., Iratni R., Erdjument-Bromage H., Tempst P., Reinberg D. Histone deacetylases and SAP18, a novel polypeptide, are components of a human Sin3 complex. Cell. 89:1997;357-364.
    • (1997) Cell , vol.89 , pp. 357-364
    • Zhang, Y.1    Iratni, R.2    Erdjument-Bromage, H.3    Tempst, P.4    Reinberg, D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.