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Wilson病11例临床分析

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出处 《云南医药》 CAS 2002年第6期469-471,共3页 Medicine and Pharmacy of Yunnan
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  • 1李采娟,左伋,陈秀珍,夏蓓莉,刘道宽.Huntington舞蹈病患者培养细胞的电镜观察及其立体分析[J]遗传与疾病,1988(03).
  • 2Martin JB,左伋.神经系统遗传性疾病的分子遗传学研究[J]国外医学.遗传学分册,1986(06).
  • 3McCormack MK,et al.A genetic study of red cell osmotic fragility in Huntington’s disease. American Journal of Medical Genetics . 1994
  • 4Martin JB.Huntington’s disease: new approaches to an old problem. Neurology . 1984
  • 5Frydman M,et al.Assignment of gene for wilson disease to chromosome 13: linkage to the esteras D locus. Proceedings of the National Academy of Sciences of the United States of America . 1985
  • 6Kunkel LM,et al.Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proceedings of the National Academy of Sciences of the United States of America . 1985
  • 7Bowcock AM,et al.Mapping the wilson disease locus to a cluster or linked polymorphic markers on chromosome 13. The American Journal of Human Genetics . 1987
  • 8Gilliam TC,et al.A DNA segment encoding two genes very tightly linked to Huntington’s disease. Science . 1987
  • 9Chan WY,et al.Genetic expression of Wilson’s disease in cell culture: a diagnostic marker. Science . 1980
  • 10Gusella JF,et al.A polymorphic DNA marker genetically linked to Huntington’s disease. Nature . 1983

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