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P20.06: The experience with whole‐genome array as a first‐line cytogenetic test in invasive prenatal diagnosis
Author(s) -
Hynek M.,
Trkova M.,
Becvarova V.,
Brezinova S.,
Smetanova D.,
Pekova H.,
Mansfeldova R.,
Koudova M.,
Horacek J.
Publication year - 2018
Publication title -
ultrasound in obstetrics and gynecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.202
H-Index - 141
eISSN - 1469-0705
pISSN - 0960-7692
DOI - 10.1002/uog.19782
Subject(s) - amniocentesis , prenatal diagnosis , medicine , chorionic villus sampling , trisomy , amniotic fluid , copy number variation , microarray , fetus , genetics , pathology , genome , biology , gene , pregnancy , gene expression
s. © The Authors 2018 © Ultrasound in Obstetrics & Gynecology 2018; 52 (Suppl. 1): 138–193. 193
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