Sarah Guterman
Paris, France
Last Updated: 09/26/2026
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Found 8 publications
COG6-related prenatal phenotype (CDG2L): Clinico-pathological report and review of the literature.
Journal: Molecular genetics & genomic medicine
Published: January 03, 2024
1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.
Journal: American journal of medical genetics. Part A
Published: December 15, 2021
Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
Journal: Prenatal diagnosis
Published: December 17, 2018
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Journal: Prenatal diagnosis
Published: November 19, 2018
Autoimmune disorders but not heparin are associated with cell-free fetal DNA test failure.
Journal: Journal of translational medicine
Published: September 17, 2018
First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.
Journal: The journal of obstetrics and gynaecology research
Published: May 05, 2017
Laparoscopy in the second and third trimesters of pregnancy for abdominal surgical emergencies.
Journal: Journal of gynecology obstetrics and human reproduction
Published: December 10, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026