换一批
换一批Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes.
作者：
主题词
青少年(Adolescent);成年人(Adult);等位基因(Alleles);儿童(Child);儿童, 学龄前(Child, Preschool);女(雌)性(Female);遗传关联研究(Genetic Association Studies);基因型(Genotype);人类(Humans);婴儿(Infant);婴儿, 新生(Infant, Newborn);核型分析(Karyotyping);男(雄)性(Male);突变(Mutation);骨髓增殖性疾病(Myeloproliferative Disorders);表型(Phenotype);真性红细胞增多症(Polycythemia Vera);多态性, 单核苷酸(Polymorphism, Single Nucleotide);原发性骨髓纤维化(Primary Myelofibrosis);阻遏蛋白质类(Repressor Proteins);血小板增多, 原发性(Thrombocythemia, Essential);血小板增多(Thrombocytosis);青年人(Young Adult)
DOI
10.3324/haematol.2011.045591
PMID
21712540
发布时间
2021-10-20
- 浏览66
Haematologica
1462-9页
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