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Maureen Kelly

Showing results (41-50 of 44) with videos related to

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Journal of Clinical Medicine|August 27, 2021
Supervised Machine Learning Approach to Identify Early Predictors of Poor Outcome in Patients with COVID-19 Presenting to a Large Quaternary Care Hospital in New York CityJason Zucker, Angela Gomez-Simmonds, Lawrence J Purpura, et al.
European Journal of Human Genetics : EJHG|June 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2023
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individualsElisabeth Bosch, Bernt Popp, Esther Güse, et al.
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Showing results (41-50 of 44) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Journal of Clinical Medicine|August 27, 2021
Supervised Machine Learning Approach to Identify Early Predictors of Poor Outcome in Patients with COVID-19 Presenting to a Large Quaternary Care Hospital in New York CityJason Zucker, Angela Gomez-Simmonds, Lawrence J Purpura, et al.
European Journal of Human Genetics : EJHG|June 14, 2025
Structural variation in nebulin and its impact on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Structural variation in nebulin and its implications on phenotype and inheritance: establishing a dominant distal phenotype caused by large deletionsLydia Sagath, Kirsi Kiiski, Kireshnee Naidu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2023
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individualsElisabeth Bosch, Bernt Popp, Esther Güse, et al.
Pageof 5