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Yves Ville

Showing results (241-250 of 253) with videos related to

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American Journal of Medical Genetics. Part A|April 23, 2018
Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomaliesCaroline Alby, Lucile Boutaud, Bettina Bessières, et al.
Journal of Gynecology Obstetrics and Human Reproduction|March 16, 2024
Maternal and neonatal outcomes of French prospective multicenter cohort study COVIPREG during the first two COVID-19 wavesAlexandre J Vivanti, Camille Couffignal, Jeanne Sibiude, et al.
European Journal of Medical Genetics|January 10, 2012
Phenotypic spectrum of fetal Smith-Lemli-Opitz syndromeChloé Quélin, Philippe Loget, Alain Verloes, et al.
Prenatal Diagnosis|June 8, 2020
Ultrasound features of fetal toxoplasmosis: A contemporary multicenter survey in 88 fetusesCamille Codaccioni, Olivier Picone, Véronique Lambert, et al.
American Journal of Human Genetics|August 14, 2012
TCTN3 mutations cause Mohr-Majewski syndromeSophie Thomas, Marine Legendre, Sophie Saunier, et al.
Clinical Genetics|July 5, 2020
Fetal megacystis-microcolon: Genetic mutational spectrum and identification of PDCL3 as a novel candidate geneClarisse Billon, Arnaud Molin, Céline Poirsier, et al.
The Lancet Regional Health. Europe|January 11, 2023
Maternal and perinatal outcomes following pre-Delta, Delta, and Omicron SARS-CoV-2 variants infection among unvaccinated pregnant women in France and Switzerland: a prospective cohort study using the COVI-PREG registryGuillaume Favre, Emeline Maisonneuve, Léo Pomar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 25, 2025
First real-world study of fetal therapy with CFTR modulators in cystic fibrosis: Report from the MODUL-CF studyAnne-Sophie Bonnel, Tiphaine Bihouée, Mélanie Ribault, et al.
Journal of Medical Genetics|October 2, 2012
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutationsMarine Legendre, Marie Gonzales, Géraldine Goudefroye, et al.
Journal of Clinical Medicine|June 11, 2020
Post-Laser Twin Anemia Polycythemia Sequence: Diagnosis, Management, and Outcome in an International Cohort of 164 CasesLisanne S A Tollenaar, Enrico Lopriore, Stefano Faiola, et al.
Pageof 26

Showing results (241-250 of 253) with videos related to

Sort By:
Pageof 26
American Journal of Medical Genetics. Part A|April 23, 2018
Novel de novo ZBTB20 mutations in three cases with Primrose syndrome and constant corpus callosum anomaliesCaroline Alby, Lucile Boutaud, Bettina Bessières, et al.
Journal of Gynecology Obstetrics and Human Reproduction|March 16, 2024
Maternal and neonatal outcomes of French prospective multicenter cohort study COVIPREG during the first two COVID-19 wavesAlexandre J Vivanti, Camille Couffignal, Jeanne Sibiude, et al.
European Journal of Medical Genetics|January 10, 2012
Phenotypic spectrum of fetal Smith-Lemli-Opitz syndromeChloé Quélin, Philippe Loget, Alain Verloes, et al.
Prenatal Diagnosis|June 8, 2020
Ultrasound features of fetal toxoplasmosis: A contemporary multicenter survey in 88 fetusesCamille Codaccioni, Olivier Picone, Véronique Lambert, et al.
American Journal of Human Genetics|August 14, 2012
TCTN3 mutations cause Mohr-Majewski syndromeSophie Thomas, Marine Legendre, Sophie Saunier, et al.
Clinical Genetics|July 5, 2020
Fetal megacystis-microcolon: Genetic mutational spectrum and identification of PDCL3 as a novel candidate geneClarisse Billon, Arnaud Molin, Céline Poirsier, et al.
The Lancet Regional Health. Europe|January 11, 2023
Maternal and perinatal outcomes following pre-Delta, Delta, and Omicron SARS-CoV-2 variants infection among unvaccinated pregnant women in France and Switzerland: a prospective cohort study using the COVI-PREG registryGuillaume Favre, Emeline Maisonneuve, Léo Pomar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 25, 2025
First real-world study of fetal therapy with CFTR modulators in cystic fibrosis: Report from the MODUL-CF studyAnne-Sophie Bonnel, Tiphaine Bihouée, Mélanie Ribault, et al.
Journal of Medical Genetics|October 2, 2012
Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutationsMarine Legendre, Marie Gonzales, Géraldine Goudefroye, et al.
Journal of Clinical Medicine|June 11, 2020
Post-Laser Twin Anemia Polycythemia Sequence: Diagnosis, Management, and Outcome in an International Cohort of 164 CasesLisanne S A Tollenaar, Enrico Lopriore, Stefano Faiola, et al.
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