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Luis Escobar

Showing results (71-80 of 74) with videos related to

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The New England Journal of Medicine|June 20, 2019
Reanalysis of Clinical Exome Sequencing DataPengfei Liu, Linyan Meng, Elizabeth A Normand, et al.
European Heart Journal|July 15, 2021
Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathyLuis R Lopes, Soledad Garcia-Hernández, Massimiliano Lorenzini, et al.
Human Mutation|July 17, 2015
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype CorrelationKitiwan Rojnueangnit, Jing Xie, Alicia Gomes, et al.
European Heart Journal|August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onsetRenee Johnson, Robert A Fletcher, Stacey Peters, et al.
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Showing results (71-80 of 74) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 74 results.
The New England Journal of Medicine|June 20, 2019
Reanalysis of Clinical Exome Sequencing DataPengfei Liu, Linyan Meng, Elizabeth A Normand, et al.
European Heart Journal|July 15, 2021
Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathyLuis R Lopes, Soledad Garcia-Hernández, Massimiliano Lorenzini, et al.
Human Mutation|July 17, 2015
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype CorrelationKitiwan Rojnueangnit, Jing Xie, Alicia Gomes, et al.
European Heart Journal|August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onsetRenee Johnson, Robert A Fletcher, Stacey Peters, et al.
Pageof 8