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American Journal of Medical Genetics. Part A|January 25, 2018
NRP1 haploinsufficiency predisposes to the development of Tetralogy of FallotIvan Duran, Jessica Tenney, Carmen M Warren, et al.
Human Molecular Genetics|December 17, 2014
HSP47 and FKBP65 cooperate in the synthesis of type I procollagenIvan Duran, Lisette Nevarez, Anna Sarukhanov, et al.
Radiology Case Reports|March 20, 2020
Personalized selective internal radiation therapy in liver metastasis of thyroid cancer with impaired liver function: A case reportMaxime Herchuelz, Gwennaëlle Marin, Ivan Duran Derijckere, et al.
BMJ Case Reports|February 25, 2026
Unexpected diagnosis of thymic small cell carcinoma following acute respiratory distressMarine Najmaoui, Sébastien Van Laethem, Nathan Blekic, et al.
Human Mutation|August 8, 2019
Dominant-negative SOX9 mutations in campomelic dysplasiaFabiana Csukasi, Ivan Duran, Wenjuan Zhang, et al.
Nature Communications|June 17, 2015
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndromeS Paige Taylor, Tiago J Dantas, Ivan Duran, et al.
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