Premium
VP25.06: Anophthalmia due to a novel mutation in the SOX2 gene
Author(s) -
Nanda M.,
Gellen J.,
Csapo B.,
Eisnecker K.,
Greimel P.,
Duba H.,
Pölsler L.,
WitschBaumgartner M.,
Kampelmuhler E.,
Klaritsch P.
Publication year - 2020
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.22717
Subject(s) - anophthalmia , medicine , agenesis of the corpus callosum , corpus callosum agenesis , anencephaly , agenesis , corpus callosum , prenatal diagnosis , pregnancy , obstetrics , pediatrics , genetics , pathology , fetus , anatomy , microphthalmia , gene , biology