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色素失禁症 被引量:1

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出处 《罕少疾病杂志》 2001年第4期60-61,共2页 Journal of Rare and Uncommon Diseases
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  • 1孙东信,临床儿科杂志,1983年,1卷,60页

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  • 1孙东信.色素失禁症38例分析[J].中华皮肤科杂志,1996,29(1):15-17. 被引量:14
  • 2Koffimann CP,Desouza DH,DiamentA,et al.Incontinentia pigmenti achromians (hpyomelanosis of ITO,MIMI 46150):furtheRevidence of localization at Xp11[J].Am J Med Genet,1993,46 (5):529.
  • 3Sefiani A,Abel L,Heuertz S,et al.The gene for incotinentia pigmenti is assigned to Xq28[J].Genomics,1989,4 (3):427.
  • 4Fusco F,Bardaro T,Fimiani G,et al.Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activation[J].Hum Mol Genet,2004,15; 13 (16):1763-1773.
  • 5Katori H,Baba Y,Irnagawa Y,et al.Reduction of in vivo tumor growth by MMI-166,a selective matrix metalloproteinase inhibitor,through inhibition of tumoRangiogenesis in squamous cell carcinoma cell lines of head and neck[J].Cancer Lett,2002,178 (2):151-159.
  • 6Basarab T,Dunnill MG,Munn SE,et al.Incontinentia pigmenti:variable disease expression within an affected family[J].Journal of the European Academy of Dermatology and Venereology,1998,11(2):173-176.
  • 7唐兰芳,邹朝春.色素失禁症临床分析[J].中华皮肤科杂志,2001,34(6):442-442. 被引量:12

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