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American Journal of Medical Genetics. Part A|February 13, 2013
Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasiaJulie Plaisancié, Isabelle Bailleul-Forestier, Véronique Gaston, et al.
The New Phytologist|December 14, 2023
Hypometabolism to survive the long polar night and subsequent successful return to light in the diatom Fragilariopsis cylindrusNathalie Joli, Lorenzo Concia, Karel Mocaer, et al.
Molecular Ecology|December 13, 2022
Stepping up to genome scan allows stock differentiation in the worldwide distributed blue shark Prionace glaucaNatacha Nikolic, Floriaan Devloo-Delva, Diane Bailleul, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 13, 2008
Southern Ocean frontal structure and sea-ice formation rates revealed by elephant sealsJ-B Charrassin, M Hindell, S R Rintoul, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2022
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defectsAuriane Cospain, Ana Rivera-Barahona, Erwan Dumontet, et al.
Human Molecular Genetics|February 12, 2015
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfectaMathilde Huckert, Corinne Stoetzel, Supawich Morkmued, et al.
ESC Heart Failure|September 8, 2021
Characteristics and outcome of ambulatory heart failure patients receiving a left ventricular assist deviceGuillaume Baudry, Nicolas Nesseler, Erwan Flecher, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|May 31, 2023
[Pelvic exam in gynecology and obstetrics: Guidelines for clinical practice]Xavier Deffieux, Christine Rousset-Jablonski, Adrien Gantois, et al.
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