Lucy Gugasyan
Clayton, VIC, Australia
Last Updated: 09/26/2026
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Found 8 publications
Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study.
Journal: Genetics in medicine open
Published: January 24, 2025
Phenotype of patients with late diagnosis of 22q11 deletion: a review and retrospective study.
Journal: Internal medicine journal
Published: February 27, 2024
Reexamining the optimal nuchal translucency cutoff for diagnostic testing in the cell-free DNA and microarray era: results from the Victorian Perinatal Record Linkage study.
Journal: American journal of obstetrics and gynecology
Published: November 29, 2020
Abstracts of the 29th World Congress on Ultrasound in Obstetrics and Gynecology, 12-16 October 2019, Berlin, Germany.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: December 05, 2019
State-wide utilization and performance of traditional and cell-free DNA-based prenatal testing pathways: the Victorian Perinatal Record Linkage (PeRL) study.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: June 28, 2019
Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016.
Journal: Prenatal diagnosis
Published: April 12, 2019
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Journal: Human reproduction (Oxford, England)
Published: December 30, 2018
Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch.
Journal: Clinical case reports
Published: March 23, 2016
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Last Updated: 09/26/2026