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Showing results (201-210 of 205) with videos related to

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Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 7, 2023
Developmental impairment in children exposed during pregnancy to maternal SARS-COV2: A Brazilian cohort studyCarolina A D Santos, Artemis P Paula, Gentil G Fonseca Filho, et al.
Clinical Endocrinology|December 7, 2000
Comparison of octreotide acetate LAR and lanreotide SR in patients with acromegalyP Chanson, V Boerlin, C Ajzenberg, et al.
American Journal of Medical Genetics. Part A|June 21, 2017
Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twinsFernanda S Jehee, Valdirene T de Oliveira, Juliana Gurgel-Giannetti, et al.
International Journal of Surgery (London, England)|November 17, 2021
Simplified risk-prediction for benchmarking and quality improvement in emergency general surgery. Prospective, multicenter, observational cohort studyC Villodre, L Taccogna, P Zapater, et al.
Pageof 21

Showing results (201-210 of 205) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 205 results.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 7, 2023
Developmental impairment in children exposed during pregnancy to maternal SARS-COV2: A Brazilian cohort studyCarolina A D Santos, Artemis P Paula, Gentil G Fonseca Filho, et al.
Clinical Endocrinology|December 7, 2000
Comparison of octreotide acetate LAR and lanreotide SR in patients with acromegalyP Chanson, V Boerlin, C Ajzenberg, et al.
American Journal of Medical Genetics. Part A|June 21, 2017
Dual molecular diagnosis contributes to atypical Prader-Willi phenotype in monozygotic twinsFernanda S Jehee, Valdirene T de Oliveira, Juliana Gurgel-Giannetti, et al.
International Journal of Surgery (London, England)|November 17, 2021
Simplified risk-prediction for benchmarking and quality improvement in emergency general surgery. Prospective, multicenter, observational cohort studyC Villodre, L Taccogna, P Zapater, et al.
Pageof 21