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EP03.07: Prenatal diagnosis of 22q11.2 microdeletion: minor cardiac finding detected in mid‐trimester scan associated with severe bilateral perisylvian polymicrogyria in late gestation
Author(s) -
Weizman B.,
Bakry H.,
Haratz K.K.,
Gindes L.,
Tamarkin M.,
Sagie S.,
Shapiro I.,
Cohen G.,
BenSira L.,
Lev D.,
LermanSagie T.,
Leibovitz Z.
Publication year - 2017
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.18345
Subject(s) - polymicrogyria , medicine , hypoplasia , autopsy , anatomy , global developmental delay , digeorge syndrome , microdeletion syndrome , agenesis , microcephaly , cardiology , pathology , radiology , pediatrics , magnetic resonance imaging , psychiatry , biochemistry , chemistry , gene , phenotype
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