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弥漫性掌跖角化病1例

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出处 《武警医学》 CAS 2007年第5期370-370,共1页 Medical Journal of the Chinese People's Armed Police Force
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参考文献2

  • 1李景卫,尹兴平,夏隆庆.弥漫性掌跖角化病[J].国外医学(皮肤性病学分册),2005,31(2):87-89. 被引量:5
  • 2Stevens HP,kel sell DP,Bryant SP et al.linkage of an American pedigree with palnroplantar keratodema and malignancy (palmoplantar ectodermal dysplasia type Ⅲ) to 17q24 Literature survery and proposed updated classification of the keratodermas.Arch Dermatol,1996,132:640

二级参考文献20

  • 1Risk JM, Ruhrberg C, Hennies H, et al. Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC) : the integration of genetic and physical maps of the TOC region on 17q25. Genomics, 1999, 59:234-242.
  • 2Maestrini E, Monaco AP, McGrath JA, et al, A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet. 1996, 13:70-77.
  • 3Takahashi H, Ishida-Yamamoto A, Kishi A, et al, Lorierin gene mutation in a Japanese patient of Vohwinkel's syndrome. J Dermatol Sei,1999, 19:44-47.
  • 4Kibar Z, Der Kaloustian VM, Brais B, et al. The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q. Hum Mol Genet, 1996, 5:543 -547.
  • 5Coonar AS, Protonotarios N, Tsatsopoulou A, et al. Gene for arrhythmogenic right ventficular cardiomyopathy with diffuse nonepidermolytic pahnoplantar keratoderma and woolly hair ( Naxos disease ) maps to 17q21. Circulation, 1998, 97:2049 - 2058.
  • 6Maillefer RH, Greydanus MP. To B or not to B : is tylosis B truly benign? Two North American genealogies. Am J Gastroenterol, 1999,94:829 - 834.
  • 7Yang JM, Lee S, Kang HJ,et al. Mutations in the 1A rod domain segment of the keratin 9 gene in epidennolytie pahnoplantar keratoderma.Acta Denn Venereol, 1998, 78:412-416.
  • 8Tsunemi Y, Hattori N, Saeki H, et al. A keratin 9 Gene mutation(Asn160Ser) in a Japanese patient with epidermolytie pahnoplantar keratoderma. J Dermatol, 2002, 29:768- 772.
  • 9Kimonis V, DiGiovanna JJ, Yang JM, et al, A mutation in the V1 end domain of keratin 1 in non-epidennolytic palmar-plantar keratoderma. J Invest Dennatol, 1994, 103:764-769.
  • 10Richard G, Smith LE, Bailey RA, et al. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat Genet,1998. 20:366 - 369.

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