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OC18.01: Use of exome sequencing in fetuses with complex central nervous system anomalies
Author(s) -
Eixarch E.,
PerezCruz M.,
Illa M.,
Monterde E.,
Masoller N.,
Pauta M.,
Martínez J.,
Gratacós E.,
Borrell A.
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.22329
Subject(s) - exome sequencing , ventriculomegaly , sanger sequencing , medicine , neural tube , microcephaly , central nervous system , exome , fetus , genetics , phenotype , anatomy , pathology , biology , mutation , gene , pregnancy , embryo , pediatrics