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European Journal of Human Genetics : EJHG|August 9, 2023
Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54Thomas B Smith, Alessandro Rea, Huw B Thomas, et al.Neurology. Genetics|October 27, 2021
Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in GPAA1Alison M R Castle, Smrithi Salian, Haim Bassan, et al.American Journal of Obstetrics and Gynecology|August 16, 2020
Levonorgestrel-releasing intrauterine system versus endometrial ablation for heavy menstrual bleedingPleun Beelen, Marian J van den Brink, Malou C Herman, et al.BMC Women'S Health|August 10, 2013
Levonorgestrel releasing intrauterine system (Mirena) versus endometrial ablation (Novasure) in women with heavy menstrual bleeding: a multicentre randomised controlled trialMalou C Herman, Marian J van den Brink, Peggy M Geomini, et al.BMC Genomics|December 5, 2021
Discovery of clinically relevant fusions in pediatric cancerStephanie LaHaye, James R Fitch, Kyle J Voytovich, et al.American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.Pageof 33