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European Journal of Medical Genetics|May 9, 2008
Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delayJoris Andrieux, Steven Richebourg, Bénédicte Duban-Bedu, et al.
European Journal of Medical Genetics|November 25, 2010
Crane-Heise syndrome: two further case reportsFlorence Petit, Louise Devisme, Annick Toutain, et al.
The Journal of Endocrinology|November 8, 2018
FSH inhibits AMH to support ovarian estradiol synthesis in infantile miceMarie M Devillers, Florence Petit, Victoria Cluzet, et al.
Biological Psychiatry|December 10, 2022
Habenular Neurons Expressing Mu Opioid Receptors Promote Negative Affect in a Projection-Specific MannerJulie Bailly, Florence Allain, Eric Schwartz, et al.
Journal of Genetic Counseling|November 1, 2016
The Subjective Experience of Patients Diagnosed with Hereditary Hemorrhagic Telangiectasia: a Qualitative StudyLaura Geerts, Carole Fantini-Hauwel, Elodie Brugallé, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 6, 2019
Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrixSarah Delbaere, Tibbe Dhooge, Delfien Syx, et al.
Joint Bone Spine|October 18, 2017
Statin use and knee osteoarthritis progression: Results from a post-hoc analysis of the SEKOIA trialFlorent Eymard, Camille Parsons, Mark H Edwards, et al.
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