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Journal of Personalized Medicine|June 2, 2021
A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel TherapyMariana Angulo-Aguado, Karen Panche, Caroll Andrea Tamayo-Agudelo, et al.Iscience|May 7, 2020
Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 IsoformsAurélien Ducat, Betty Couderc, Anthony Bouter, et al.Human Mutation|July 22, 2008
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndromeDiane Beysen, Sarah De Jaegere, David Amor, et al.Human Mutation|May 4, 2012
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosisChristine P Diggle, David A Parry, Clare V Logan, et al.Pageof 7