The implications of the cloning of the XLA gene.
作者信息
Flinter F A, Vetrie D, Bobrow M
机构信息
South East Thames Regional Genetics Centre, Guy's Hospital, London.
出版信息
J R Coll Physicians Lond. 1993 Jul;27(3):233-5.
Abstract
摘要
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Agammaglobulinemia.无丙种球蛋白血症
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Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22.遗传连锁分析确定了X连锁无丙种球蛋白血症基因座新的近端和远端侧翼标记，将其定位精确到Xq22。
Hum Mol Genet. 1993 Feb;2(2):139-41. doi: 10.1093/hmg/2.2.139.
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Primary hypogammaglobulinaemia: a survey of clinical manifestations and complications.原发性低丙种球蛋白血症：临床表现及并发症调查
Q J Med. 1993 Jan;86(1):31-42.
4
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.与X连锁无丙种球蛋白血症相关的基因是蛋白质酪氨酸激酶src家族的成员。
Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0.
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Construction of a 5.2-megabase physical map of the human X chromosome at Xq22 using pulsed-field gel electrophoresis and yeast artificial chromosomes.利用脉冲场凝胶电泳和酵母人工染色体构建人类X染色体Xq22区域的5.2兆碱基物理图谱。
Genomics. 1993 Mar;15(3):631-42. doi: 10.1006/geno.1993.1118.
6
Expression of the gene defect in X-linked agammaglobulinemia.X连锁无丙种球蛋白血症中基因缺陷的表达。
N Engl J Med. 1986 Aug 28;315(9):564-7. doi: 10.1056/NEJM198608283150907.
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Genetic prediction in X-linked agammaglobulinaemia.
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