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Michael Yates

Showing results (11-20 of 15) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2018
SLC35A2-related congenital disorder of glycosylation: Defining the phenotypeT Michael Yates, Mohnish Suri, Archana Desurkar, et al.
Annals of Surgery|June 23, 2022
Potential Clinical Utility of a Targeted Circulating Tumor DNA Assay in Esophageal AdenocarcinomaCarlos S Cabalag, Michael Yates, Mariana Benitez Corrales, et al.
Journal of Molecular Biology|March 28, 2026
Gene2Phenotype: a database of structured human monogenic diseases and pathomechanismsSarah E Hunt, Diana Lemos, Seeta Ramaraju Pericherla, et al.
Clinical Genetics|July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorderStephanie Oates, Michael Absoud, Sushma Goyal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2022
The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resourcesMarina T DiStefano, Scott Goehringer, Lawrence Babb, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2018
SLC35A2-related congenital disorder of glycosylation: Defining the phenotypeT Michael Yates, Mohnish Suri, Archana Desurkar, et al.
Annals of Surgery|June 23, 2022
Potential Clinical Utility of a Targeted Circulating Tumor DNA Assay in Esophageal AdenocarcinomaCarlos S Cabalag, Michael Yates, Mariana Benitez Corrales, et al.
Journal of Molecular Biology|March 28, 2026
Gene2Phenotype: a database of structured human monogenic diseases and pathomechanismsSarah E Hunt, Diana Lemos, Seeta Ramaraju Pericherla, et al.
Clinical Genetics|July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorderStephanie Oates, Michael Absoud, Sushma Goyal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2022
The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resourcesMarina T DiStefano, Scott Goehringer, Lawrence Babb, et al.
Pageof 2