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Ammar Husami

Showing results (21-30 of 41) with videos related to

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Plos One|November 1, 2018
Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitisMaisam Abu-El-Haija, Lindsey Hornung, Lee A Denson, et al.
Pediatric Pulmonology|October 11, 2023
A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptomsJesun Lee, Ammar Husami, Kavisha Arora, et al.
The Journal of Infectious Diseases|November 25, 2015
Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 InfluenzaGrant S Schulert, Mingce Zhang, Ndate Fall, et al.
American Journal of Medical Genetics. Part A|October 8, 2022
PPP2R1A neurodevelopmental disorder is associated with congenital heart defectsElizabeth K Baker, Beulah Solivio, Ben Pode-Shakked, et al.
BMC Bioinformatics|March 3, 2021
vcf2fhir: a utility to convert VCF files into HL7 FHIR format for genomics-EHR integrationRobert H Dolin, Shaileshbhai R Gothi, Aziz Boxwala, et al.
Frontiers in Genetics|February 28, 2014
The struggle to find reliable results in exome sequencing data: filtering out Mendelian errorsZubin H Patel, Leah C Kottyan, Sara Lazaro, et al.
Gastroenterology|March 27, 2021
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model OrganismsDuc-Hung Pham, Ramesh Kudira, Lingfen Xu, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|August 6, 2019
Systemic Juvenile Idiopathic Arthritis-Associated Lung Disease: Characterization and Risk FactorsGrant S Schulert, Shima Yasin, Brenna Carey, et al.
Journal of the American Medical Informatics Association : JAMIA|December 22, 2022
Introducing HL7 FHIR Genomics Operations: a developer-friendly approach to genomics-EHR integrationRobert H Dolin, Bret S E Heale, Gil Alterovitz, et al.
Haematologica|October 6, 2022
Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type IIIGonzalo Hernández, Lídia Romero-Cortadellas, Xènia Ferrer-Cortès, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Plos One|November 1, 2018
Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitisMaisam Abu-El-Haija, Lindsey Hornung, Lee A Denson, et al.
Pediatric Pulmonology|October 11, 2023
A personalized medicine approach to optimize care for a pediatric cystic fibrosis patient with atypical clinical symptomsJesun Lee, Ammar Husami, Kavisha Arora, et al.
The Journal of Infectious Diseases|November 25, 2015
Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 InfluenzaGrant S Schulert, Mingce Zhang, Ndate Fall, et al.
American Journal of Medical Genetics. Part A|October 8, 2022
PPP2R1A neurodevelopmental disorder is associated with congenital heart defectsElizabeth K Baker, Beulah Solivio, Ben Pode-Shakked, et al.
BMC Bioinformatics|March 3, 2021
vcf2fhir: a utility to convert VCF files into HL7 FHIR format for genomics-EHR integrationRobert H Dolin, Shaileshbhai R Gothi, Aziz Boxwala, et al.
Frontiers in Genetics|February 28, 2014
The struggle to find reliable results in exome sequencing data: filtering out Mendelian errorsZubin H Patel, Leah C Kottyan, Sara Lazaro, et al.
Gastroenterology|March 27, 2021
Deleterious Variants in ABCC12 are Detected in Idiopathic Chronic Cholestasis and Cause Intrahepatic Bile Duct Loss in Model OrganismsDuc-Hung Pham, Ramesh Kudira, Lingfen Xu, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|August 6, 2019
Systemic Juvenile Idiopathic Arthritis-Associated Lung Disease: Characterization and Risk FactorsGrant S Schulert, Shima Yasin, Brenna Carey, et al.
Journal of the American Medical Informatics Association : JAMIA|December 22, 2022
Introducing HL7 FHIR Genomics Operations: a developer-friendly approach to genomics-EHR integrationRobert H Dolin, Bret S E Heale, Gil Alterovitz, et al.
Haematologica|October 6, 2022
Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type IIIGonzalo Hernández, Lídia Romero-Cortadellas, Xènia Ferrer-Cortès, et al.
Pageof 5