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Prenatal diagnosis of pontocerebellar hypoplasia associated with rare syndromes: expanding the genetic and phenotypic spectrum
Author(s) -
Desai S.,
Desai T.
Publication year - 2021
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.22038
Subject(s) - medicine , hypoplasia , anatomy , agenesis , cerebellar hypoplasia (non human) , single umbilical artery , fetus , pregnancy , cerebellum , genetics , biology