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American Journal of Medical Genetics. Part A|March 16, 2012
Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformationsVéronique Haddad, Azzedine Aboura, Lucie Tosca, et al.
Fertility and Sterility|September 3, 2017
New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian familyNouha Bouali, Bruno Francou, Jérôme Bouligand, et al.
Scientific Reports|September 14, 2024
Improved functionality of hepatic spheroids cultured in acoustic levitation compared to existing 2D and 3D modelsLucile Rabiet, Nathan Jeger-Madiot, Duván Rojas García, et al.
Molecular Cytogenetics|February 12, 2015
Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent diseaseNarjes Armanet, Corinne Metay, Sophie Brisset, et al.
Prenatal Diagnosis|November 20, 2022
Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic herniaMarie Boisson, Anne-Gael Cordier, Jelena Martinovic, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 3, 2016
Confined blood chimerism in a monochorionic dizygotic sex discordant twin pregnancy conceived after induced ovulationAnne Mayeur Le Bras, François Petit, Alexandra Benachi, et al.
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