The implication of ‘unknown significance’ variants in next‐generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosine kinase 2 ( TYK2 TYK2 ) gene

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The implication of ‘unknown significance’ variants in next‐generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosine kinase 2 ( TYK2 TYK2 ) gene

机译：“未知意义”变体在诊断和供体选择中的下一代测序中的含义对同种异体血包膜干细胞移植的诊断和供体选择。酪氨酸激酶2（TYK2 TYK2）基因多态性骨髓增生综合征的报告（TYK2 TYK2）基因

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《British Journal of Haematology》 |2020年第4期|共3页
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中图分类血液及淋巴系疾病;
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1. The implication of ‘unknown significance’ variants in next‐generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosine kinase 2 ( TYK2 TYK2 ) gene [J] . British Journal of Haematology . 2020,第4期

机译：“未知意义”变体在诊断和供体选择中的下一代测序中的含义对同种异体血包膜干细胞移植的诊断和供体选择。酪氨酸激酶2（TYK2 TYK2）基因多态性骨髓增生综合征的报告（TYK2 TYK2）基因
2. Lack of association between tyrosine kinase 2 (TYK2) gene polymorphisms and susceptibility to SLE in a Japanese population. [J] . Kyogoku C, Morinobu A, Nishimura K, Modern rheumatology . 2009,第4期

机译：酪氨酸激酶2（TYK2）基因多态性与日本人群对SLE的敏感性之间缺乏关联。
3. Association of polymorphisms across the tyrosine kinase gene, TYK2 in UK SLE families [J] . D. S. C. Graham M. Akil, and T. J. Vyse Rheumatology . 2007,第6期

机译：酪氨酸激酶基因TYK2的多态性与英国SLE家族的关系
4. Predictive Efficacy of Low Burden EGFR Mutation Detected by Next-Generation Sequencing on Response to EGFR Tyrosine Kinase Inhibitors in Non-Small-Cell Lung Carcinoma [C] . Yeul Hong Kim, Hye Sook Kim, Jae Sook Sung, Molecular Medicine TRI-CON. . 2014

机译：下一代测序对非小细胞肺癌抗蛋白酶激酶抑制剂进行下一代测序检测的低负荷EGFR突变的预测疗效
5. Case Report: Late Onset of Myelodysplastic Syndrome From Donor Progenitor Cells After Allogeneic Stem Cell Transplantation. Which Lessons Can We Draw From the Reported Case? [O] . Mirko Farina, Simona Bernardi, Lisa Gandolfi, 2020

机译：病例报告：异构干细胞移植后供体祖细胞骨髓增生综合征的晚期发作。我们可以从报告的情况下抽取哪些课程？
6. The implication of ‘unknown significance’ variants in next‐generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosine kinase 2 ( TYK2 ) gene [O] . Bernardo López‐Andrade, Leyre Bento, Maria Diez Campelo, 2020

机译：“未知意义”变体在诊断和供体选择中的下一代测序中的含义对同种异体血包膜干细胞移植的诊断和供体选择。酪氨酸激酶2（Tyk2）基因多态性骨髓增生术综合征的报告

The implication of ‘unknown significance’ variants in next‐generation sequencing in diagnosis and donor selection for allogenic haematopoietic stem cell transplantation. Report of a case of myelodysplastic syndrome with a polymorphism in the tyrosine kinase 2 ( TYK2 TYK2 ) gene

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