Utility of whole-genome sequencing in the clinical diagnostic of rare inherited anaemias

被引：0

作者：

Camps, C. ^{[1
,2
]}

Roy, N. B. A. ^{[3
,4
]}

Dreau, H. ^{[3
]}

Henderson, S. ^{[3
]}

Knight, S. J. L. ^{[1
,2
]}

Kvikstad, E. M. ^{[1
,2
]}

Pentony, M. M. ^{[1
,2
]}

Proven, M. ^{[3
]}

Schuh, A. ^{[3
]}

Taylor, J. C. ^{[1
,2
]}

机构：

[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England

[2] NIHR, Comprehens Biomed Res Ctr, Oxford, England

[3] John Radcliffe Hosp, BRC Blood Theme & BRC NHS Translat Mol Diagnost C, Oxford, England

[4] Weatherall Inst Mol Med, Mol Haematol Unit, Oxford, England

来源：

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P14.097A

引用

页码：675 / 676

页数：2

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