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Sebastian综合征四例 被引量:4

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出处 《中华血液学杂志》 CAS CSCD 北大核心 2004年第3期192-192,共1页 Chinese Journal of Hematology
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同被引文献47

  • 1邵秀茹,李家增,马军,展昭民,梁红,佘袭楠,鲁海玲,王来慈,贾垂明,吴丽洁,靳明华,陈立君.一例May-Hegglin异常家系临床及分子生物学研究[J].中华血液学杂志,2004,25(9):548-551. 被引量:17
  • 2丛玉隆,金大鸣,王鸿利,冈田德弘,彭作辉,中国人群成人静脉血细胞分析参考范围调查协作组.中国人群成人静脉血细胞分析参考范围调查[J].中华医学杂志,2003,83(14):1201-1205. 被引量:177
  • 3杨海燕,王兆钺.MYH9综合征的免疫荧光检测与基因分析[J].苏州大学学报(医学版),2006,26(6):973-976. 被引量:9
  • 4杨海燕,王兆钺,苏雁华,曹丽娟,白霞,阮长耿.一例Fechtner综合征临床与分子缺陷研究——附文献复习[J].中华血液学杂志,2007,28(3):160-164. 被引量:8
  • 5Yi Y,Zhang GS, Xu M, et al. Analysis of clinical manifestations, mutant gene and encoded protein in two Chinese MYH9-related disease families. Clinica Chimica Acta, 2006,373:49-54.
  • 6Arrondel C,Vodovar N, Knebehnann B, et al. Expression of the nonmuscle myosin heavy chain ⅡA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes. J Am Soc Nephrol, 2002, 13:65-74.
  • 7Heath KE, Campos-Barros A, Toren A, et al. Nonmuscle myosin heavy chain Ⅱ A mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am J Hum Genet, 2001, 69: 1033-1045.
  • 8Seri M, Pecci A, Di Bari F,et al. MYH9- related disease May- Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distincl entities but represent a variable expression of a single illness. Medicine( Baltimore), 2003, 82 : 203 -215.
  • 9Seri M, Cusano R, Gangarossa S, et al. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. Nat Genet,2000, 26 : 103-105.
  • 10张之南.血液病学[M].北京:人民卫生出版社,2003.1101-1106.

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