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Biology of Reproduction|July 31, 2022
Genomic testing in premature ovarian insufficiency: proceed with cautionElena J Tucker, Tiong Y Tan, Zornitza Stark, et al.NPJ Genomic Medicine|July 14, 2018
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseasesMichelle M Clark, Zornitza Stark, Lauge Farnaes, et al.American Journal of Medical Genetics. Part A|June 11, 2015
SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic herniaZornitza Stark, Joanna Behrsin, Trent Burgess, et al.Endocrine Reviews|October 4, 2016
Premature Ovarian Insufficiency: New Perspectives on Genetic Cause and Phenotypic SpectrumElena J Tucker, Sonia R Grover, Anne Bachelot, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2018
Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectivenessZornitza Stark, Deborah Schofield, Melissa Martyn, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2022
Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and childrenIlias Goranitis, You Wu, Sebastian Lunke, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectivenessZornitza Stark, Deborah Schofield, Melissa Martyn, et al.European Journal of Human Genetics : EJHG|November 8, 2021
Rapid genomic testing for critically ill children: time to become standard of care?Zornitza Stark, Sian EllardNature Reviews. Disease Primers|September 12, 2024
Premature ovarian insufficiencyPhilippe Touraine, Nathalie Chabbert-Buffet, Genevieve Plu-Bureau, et al.Pageof 42