Non-Invasive Prenatal Testing pitfalls: exceptional report of multiple discrepancies between noninvasive screening for fetal trisomy 21, karyotype, array CGH and fetal ultrasound

被引：0
|
作者：
Kundul, F. [1 ,2 ]
Cassinari, K. [1 ,2 ]
Joly-Helas, G. [1 ,2 ]
Le Meur, N. [1 ,2 ]
Coursimault, J. [1 ,2 ]
Castelain, M. [1 ,2 ]
Diguet, A. [3 ]
Verspyck, E. [3 ]
Torre, S. [4 ]
Mace, B. [1 ,2 ]
Frebourg, T. [1 ,2 ]
Chambon, P. [1 ,2 ]
机构：
[1] Normandie Univ, UNIROUEN, Inserm U1245, F-76000 Rouen, France
[2] Rouen Univ Hosp, Dept Genet, Normandy Ctr Genom & Personalized Med, F-76000 Rouen, France
[3] Rouen Univ Hosp Charles Nicolle, Dept Gynecol & Obstet, Rouen, France
[4] Rouen Univ Hosp, Dept Neonatal Pediat Intens Care & Neuropediat, Rouen, France
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
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：
P01.49A
引用
收藏
页码：1195 / 1196
页数：2
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