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OC21.02: The incidence of genetic variants in fetuses with severe congenital heart defects
Author(s) -
Nisselrooij A.,
Lugthart M.,
Santen G.,
Aten E.,
Clur S.B.,
Linskens I.,
Pajkrt E.,
Rammeloo L.,
Van Lith J.,
Blom N.,
Haak M.C.
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.20567
Subject(s) - medicine , incidence (geometry) , pulmonary atresia , noonan syndrome , genetic testing , clinical significance , genetic counseling , prenatal diagnosis , fetus , medical genetics , heart disease , pediatrics , down syndrome , heart septal defect , pregnancy , genetics , biology , gene , physics , optics , psychiatry
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