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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 anomalies
Caroline 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 waves
Alexandre J Vivanti, Camille Couffignal, Jeanne Sibiude, et al.
European Journal of Medical Genetics
|
January 10, 2012
Phenotypic spectrum of fetal Smith-Lemli-Opitz syndrome
Chloé Quélin, Philippe Loget, Alain Verloes, et al.
Prenatal Diagnosis
|
June 8, 2020
Ultrasound features of fetal toxoplasmosis: A contemporary multicenter survey in 88 fetuses
Camille Codaccioni, Olivier Picone, Véronique Lambert, et al.
American Journal of Human Genetics
|
August 14, 2012
TCTN3 mutations cause Mohr-Majewski syndrome
Sophie 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 gene
Clarisse 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 registry
Guillaume 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 study
Anne-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 mutations
Marine 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 Cases
Lisanne S A Tollenaar, Enrico Lopriore, Stefano Faiola, et al.
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of 26
Search research articles
Search
Showing results (241-250 of 253) with videos related to
Sort By:
Page
of 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 anomalies
Caroline 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 waves
Alexandre J Vivanti, Camille Couffignal, Jeanne Sibiude, et al.
European Journal of Medical Genetics
|
January 10, 2012
Phenotypic spectrum of fetal Smith-Lemli-Opitz syndrome
Chloé Quélin, Philippe Loget, Alain Verloes, et al.
Prenatal Diagnosis
|
June 8, 2020
Ultrasound features of fetal toxoplasmosis: A contemporary multicenter survey in 88 fetuses
Camille Codaccioni, Olivier Picone, Véronique Lambert, et al.
American Journal of Human Genetics
|
August 14, 2012
TCTN3 mutations cause Mohr-Majewski syndrome
Sophie 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 gene
Clarisse 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 registry
Guillaume 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 study
Anne-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 mutations
Marine 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 Cases
Lisanne S A Tollenaar, Enrico Lopriore, Stefano Faiola, et al.
Page
of 26