Olivia Martz
Dijon, France
Last Updated: 09/26/2026
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Found 8 publications
The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome-SHS.
Journal: Prenatal diagnosis
Published: October 10, 2024
First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende-Gupta and 22q11.2 Deletion Syndromes.
Journal: Molecular genetics & genomic medicine
Published: August 27, 2024
Polypoid endometriosis-An exceptional subtype of endometriosis mimicking an aggressive pelvic cancer.
Journal: Clinical case reports
Published: March 16, 2024
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not?
Journal: Prenatal diagnosis
Published: July 27, 2023
Case report: Umbilical vessel aneurysm thrombosis and factor V Leiden mutation leading to fetal demise.
Journal: Frontiers in medicine
Published: October 29, 2022
Discussion of the medico legal aspects of an unusual request for pregnancy termination
Journal: Gynecologie, obstetrique, fertilite & senologie
Published: March 17, 2017
Customized and non-customized live-born birth-weight curves of single and uncomplicated pregnancies from the Burgundy perinatal network. Part I - methodology.
Journal: Journal of gynecology obstetrics and human reproduction
Published: February 10, 2017
Induced labour at term and breech presentation: Experience of a level IIB French maternity.
Journal: Journal of gynecology obstetrics and human reproduction
Published: July 10, 2016
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Last Updated: 09/26/2026