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OC02.05: What is the chance for pathogenic chromosomal microarray analysis results in structurally normal fetuses?
Author(s) -
Daum H.,
Stern S.,
Meiner V.,
Yagel S.,
Zenvirt S.,
ShkediRafid S.,
Macrov M.,
Valsky D.V.,
Porat S.,
Yanai N.,
Frumkin A.
Publication year - 2019
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.20433
Subject(s) - penetrance , medicine , fetus , pregnancy , prenatal diagnosis , genetic testing , cohort , obstetrics , microarray , copy number variation , bioinformatics , genetics , pathology , phenotype , gene , genome , biology , gene expression
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