Nathalie Roux
Paris, France
Last Updated: 09/26/2026
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Found 22 publications
Fetal density evolution and association with ultrasonographically estimated fetal weight: prospective study.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: February 09, 2025
Normative range of MRI-derived fetal brain volume throughout gestation: a prospective study.
Journal: Archives of disease in childhood. Fetal and neonatal edition
Published: February 05, 2025
Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliogenesis.
Journal: European journal of human genetics : EJHG
Published: August 22, 2024
Normative range of MRI-based fetal body volume and association with ultrasonographically estimated fetal weight at 16-36 weeks: prospective study.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: April 12, 2024
Artificial intelligence-based diagnosis in fetal pathology using external ear shapes.
Journal: Prenatal diagnosis
Published: October 22, 2023
Prenatal diagnosis of SLC25A24 Fontaine progeroid syndrome: description of the fetal phenotype, genotype and detection of parental mosaicism.
Journal: Birth defects research
Published: June 22, 2023
SARS-CoV-2 infection as cause of in-utero fetal death: regional multicenter cohort study.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: May 02, 2023
Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis.
Journal: Journal of medical genetics
Published: March 23, 2023
Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla.
Journal: Acta neuropathologica communications
Published: December 17, 2022
Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1.
Journal: Birth defects research
Published: November 22, 2022
Diagnostic value of fetal autopsy after early termination of pregnancy for fetal anomalies.
Journal: PloS one
Published: March 30, 2022
Biallelic THOC6 pathogenic variants: Prenatal phenotype and review of the literature.
Journal: Birth defects research
Published: August 28, 2021
Last Updated: 09/26/2026