Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis

被引：3

作者：

Chitty, Lyn S. ^{[1
,2
]}

van den Veyver, Ignatia B. ^{[3
,4
,5
]}

机构：

[1] Great Ormond St NHS Fdn Trust, North Thames Genom Lab Hub, London, England

[2] UCL Great Ormond St Inst Child Hlth, Genet & Genom, London, England

[3] Baylor Coll Med, Dept Obstet & Gynecol, Houston, TX 77030 USA

[4] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

[5] Texas Childrens Hosp, Houston, TX 77030 USA

来源：

PRENATAL DIAGNOSIS | 2022年 / 42卷 / 12期

关键词：

D O I：

10.1002/pd.6252

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：1479 / 1480

页数：2

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