Kolexia
Bourgon Nicolas Gynécologie
Bourgon Nicolas
Gynécologie
Hôpital Necker Enfants Malades
Paris, France
54 Activités
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{{person.topmesh1.name}} Malformations Syndrome de transfusion foeto-foetale Complications infectieuses de la grossesse Infections à cytomégalovirus Malformations multiples Maladies transmissibles Maladies virales Mésothéliome kystique Maladies foetales

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Olivier-Faivre Laurence
Olivier-Faivre Laurence
Hôpital François Mitterrand, Dijon, France
Thauvin-Robinet Christel
Thauvin-Robinet Christel
Hôpital François Mitterrand, Dijon, France
Ville Yves
Ville Yves
Hôpital Necker Enfants Malades, Paris, France
Stirnemann Julien
Stirnemann Julien
Hôpital Necker Enfants Malades, Paris, France

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Dernières activités

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Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct.
European journal of human genetics : EJHG   13 février 2024
Genomic newborn screening in France: from a social acceptability study to a pilot project
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Prospective reanalysis of unsolved prenatal exome sequencing for structural defects: feasibility and diagnostic yield
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Prenatal exome sequencing, a powerful tool to describe unreported prenatal features of monogenic disorders
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Neu Laxova syndrome and megacystis in the first trimester: Broadening the fetal phenotype.
Prenatal diagnosis   14 novembre 2023
Palaeoenvironments and hominin evolutionary dynamics in southeast Asia.
Scientific reports   27 septembre 2023
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndrome.
American journal of medical genetics. Part A   12 septembre 2023
Diagnosis of Menke-Hennekam syndrome by prenatal whole exome sequencing and review of prenatal signs.
Molecular genetics & genomic medicine   23 juin 2023
Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic tool.
Frontiers in genetics   23 mars 2023
BIO-CCMV: Biomarkers of Fetal Infection and Disease Following Maternal HCMV Infection
Essai Clinique (Assistance publique – Hôpitaux de Paris)   04 novembre 2022