首页> 外文OA文献 >Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia

【2h】

Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia

机译：最近在遗传骨髓衰竭综合征FANCONI贫血的分子发病机制中发现

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Nicholas E. Mamrak; Akiko Shimamura; Niall G. Howlett;
展开▼
作者单位

展开▼
年度 2017
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia [J] . Mamrak Nicholas E., Shimamura Akiko, Howlett Niall G. Blood reviews . 2017,第3期

机译：最近在遗传骨髓衰竭综合征FANCONI贫血的分子发病机制中发现
2. Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromes [J] . Kalejaiye Adedoyin, Giri Neelam, Brewer Carmen C., Pediatric blood & cancer . 2016,第12期

机译：范可尼贫血和其他遗传性骨髓衰竭综合征的耳部表现
3. Comparison of Chromosome Breakage in Non-Mosaic and Mosaic Patients with Fanconi Anemia, Relatives, and Patients with Other Inherited Bone Marrow Failure Syndromes [J] . Fargo John H., Rochowski Andrzej, Giri Neelam, Cytogenetic and genome research . 2014,第1期

机译：Fanosa贫血，亲戚和其他遗传性骨髓衰竭综合征患者的非镶嵌和镶嵌患者染色体断裂的比较
4. Diagnostic Value of p53 Tumor Suppressor Gene as Bone Marrow Cell Cycle Marker in Egyptian Children with Inherited Anemia [C] . Attia F., Abo-Elwafa H., Hassoba H., European Congress of Immunology . 2009

机译：P53肿瘤抑制基因作为埃及血症血症儿童骨髓细胞周期标记的诊断价值
5. Genomics of inherited bone marrow failure and myelodysplasia [D] . Zhang, Michael Yu 2015

机译：遗传性骨髓衰竭和骨髓增生异常的基因组学
6. Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia [O] . Nicholas E. Mamrak, Akiko Shimamura, Niall G. Howlett -1

机译：遗传性骨髓衰竭综合征范可尼贫血的分子发病机制的最新发现
7. Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry [O] . Tamary, Hannah, Nishri, Daniella, Yacobovich, Joanne, 2010

机译：遗传性骨髓衰竭综合征的频率和自然史：以色列遗传性骨髓衰竭登记处
8. Biochemical Approach to Understanding the Fanconi Anemia Pathway- Regulated Nucleases in Genome Maintenance for Preventing Bone Marrow Failure and Cancer [R] . Wang, A 2014

机译：生化方法了解Fanconi贫血途径调控核酸酶在基因组维护中预防骨髓衰竭和癌症

Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia

著录项

引文网络

相似文献

相关主题

期刊订阅