A method for noninvasive prenatal diagnosis of monogenic autosomal recessive disorders

被引：8
|
作者：
Cutts, Anthony [1 ,2 ,3 ]
Vavoulis, Dimitrios V. [1 ,2 ,3 ,4 ]
Petrou, Mary [5 ,6 ]
Smith, Frances [7 ]
Clark, Barnaby [8 ,9 ]
Henderson, Shirley [10 ,11 ]
Schuh, Anna [1 ,2 ,3 ,12 ]
机构：
[1] Univ Oxford, Dept Oncol, Mol Diagnost Ctr, Oxford, England
[2] Univ Oxford, NIHR Oxford Biomed Res Ctr, Oxford, England
[3] Univ Oxford, Dept Oncol, Oxford, England
[4] Univ Oxford, Wellcome Ctr Human Genet, Oxford, England
[5] UCL, Inst Womens Hlth, London, England
[6] Univ Coll London Hosp NHS Trust, Haemoglobinopathy Genet Serv, London, England
[7] Kings Coll Hosp London, Viapath LLP, Mol Diagnost, London, England
[8] Kings Coll London, Red Cell Biol, London, England
[9] Kings Coll Hosp London, Precis Med, London, England
[10] Genom England, London, England
[11] NHS England, London, England
[12] Oxford Univ Hosp NHS Trust, Dept Hematol, Oxford, England
来源：
BLOOD | 2019年 / 134卷 / 14期
关键词：
MATERNAL PLASMA; BETA-THALASSEMIA; FETAL DNA;
D O I：
10.1182/blood.2019002099
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：1190 / 1193
页数：4
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