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OP06.05: The usefulness of prenatal imaging features in discovering pathogenic genomic variations in fetal agenesis of corpus callosum
Author(s) -
Yang Y.,
Chen X.,
Yang X.,
Zhao S.,
Xia W.,
Yang F.,
Guo J.,
Cheng L.
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.19438
Subject(s) - agenesis of the corpus callosum , holoprosencephaly , corpus callosum agenesis , prenatal diagnosis , corpus callosum , missense mutation , medicine , genetics , etiology , mendelian inheritance , fetus , mutation , bioinformatics , pathology , biology , gene , pregnancy
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