Whole genome sequencing of patients with haematological, immune and haemostatic disorders reveals hundreds of new variants in the coding and non-coding part of the genome causal of rare diseases

被引：0
|
作者：
Sivapalaratnam, S. [1 ]
Lentaigne, C. [2 ]
Turro, E. [3 ]
机构：
[1] Blizard Inst, Immunobiol, London, England
[2] Imperial Coll NHS Healthcare Trust, Haematol, London, England
[3] Univ Cambridge, Haematol, Cambridge, England
来源：
BRITISH JOURNAL OF HAEMATOLOGY | 2019年 / 185卷
关键词：
100.000; genomes; HPO; Regulatory Elements; Whole Genome Sequencing;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
BSH19-OR-0
引用
收藏
页码：31 / 31
页数：1
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