Eini Westenius (E Westenius)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 5

Top Topics

Gestational Age

Contrast Enhanced Ultrasound

Top Venues

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology

Molecular cytogenetics

This page only lists publications with an associated author ORCID identifier.

Publications

Eini Westenius, P Conner, M Pettersson, E Sahlin, N Papadogiannakis, A Lindstrand, Erik Iwarsson
Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2024)
Eini Westenius, P Conner, M Pettersson, E Sahlin, N Papadogiannakis, A Lindstrand, Erik Iwarsson
Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2024)
Eini Westenius, P Conner, M Pettersson, E Sahlin, N Papadogiannakis, A Lindstrand, Erik Iwarsson
Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 63 (5) (2024)
Eini Westenius, E Sahlin, P Conner, A Lindstrand, Erik Iwarsson
Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 60 (4) (2022)
Eini Westenius, Maria Pettersson, Erik Björck
Discordant structural chromosomal aberrations in chorionic villi and amniotic fluid leading to a formation of an isochromosome 21: a case report. Molecular cytogenetics 14 (1) (2021)