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Journal of Community Genetics|September 14, 2018
Historical overview of development in methods to estimate burden of disease due to congenital disordersBernadette Modell, Matthew W Darlison, Joy E LawnStudies in Health Technology and Informatics|January 4, 2018
Developing the First Generally-Available openEHR Archetypes and Templates for Physiotherapy: An Example of Building Clinical Models and Modelling Capacity via Student-Led Academic-Industrial CollaborationJamila Chihab, Hildegard Franke, Ian McNicoll, et al.Journal of Community Genetics|March 18, 2018
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disordersHannah Blencowe, Sowmiya Moorthie, Matthew W Darlison, et al.Annals of the New York Academy of Sciences|January 25, 2018
Estimates of global and regional prevalence of neural tube defects for 2015: a systematic analysisHannah Blencowe, Vijaya Kancherla, Sowmiya Moorthie, et al.Journal of Community Genetics|March 6, 2021
Modelled epidemiological data for selected congenital disorders in South AfricaHelen L Malherbe, Colleen Aldous, Arnold L Christianson, et al.Journal of Community Genetics|October 13, 2017
An overview of concepts and approaches used in estimating the burden of congenital disorders globallySowmiya Moorthie, Hannah Blencowe, Matthew W Darlison, et al.Journal of Community Genetics|September 27, 2017
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwideSowmiya Moorthie, Hannah Blencowe, Matthew W Darlison, et al.Human Mutation|May 30, 2009
The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variationAnthony J Brookes, Heikki Lehvaslaiho, Juha Muilu, et al.Journal of Community Genetics|September 16, 2018
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwideSowmiya Moorthie, Hannah Blencowe, Matthew W Darlison, et al.Pageof 1