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P01.08: The 22q11 microdeletion syndrome: a review of prenatal ultrasonographic findings and the relation with diagnostic prenatal testing
Author(s) -
Sarac Sivrikoz T.,
Kalelioglu I.,
Has R.,
Basaran S.,
Yuksel A.
Publication year - 2016
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.16502
Subject(s) - medicine , digeorge syndrome , prenatal diagnosis , microdeletion syndrome , truncus arteriosus , hypoplasia , fluorescence in situ hybridization , pediatrics , fetus , heart disease , pregnancy , pathology , chromosome , genetics , tetralogy of fallot , gene , biology , psychiatry
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