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E Heath

Showing results (371-380 of 431) with videos related to

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Blood Cancer Discovery|January 12, 2022
Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid LeukemiaAllegra A Petti, Saad M Khan, Ziheng Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short statureAlfonso Hisado-Oliva, Alba Ruzafa-Martin, Lucia Sentchordi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 21, 2017
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone TherapyGabriela A Vasques, Mariana F A Funari, Frederico M Ferreira, et al.
Clinical Genetics|April 30, 2023
Evolution of clinical and radiological presentations of spondyloepimetaphyseal dysplasia, RPL13-related: Description of 11 further casesFrancisca Díaz-González, Manuel Parrón-Pajares, Elsa Lucas-Castro, et al.
Journal of Hematology & Oncology|February 19, 2013
A double-blind, randomized, multicenter phase 2 study of prasugrel versus placebo in adult patients with sickle cell diseaseTed Wun, Denis Soulieres, Andrew L Frelinger, et al.
American Journal of Human Genetics|September 22, 2005
A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosisSara Benito-Sanz, N Simon Thomas, Céline Huber, et al.
Journal of Medical Genetics|October 27, 2020
Biallelic cGMP-dependent type II protein kinase gene (<i>PRKG2</i>) variants cause a novel acromesomelic dysplasiaFrancisca Díaz-González, Saruchi Wadhwa, Maria Rodriguez-Zabala, et al.
Revista Espanola De Cardiologia (English Ed.)|November 18, 2017
In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular PhenotypeLuis Fernández, Jair Tenorio, Coral Polo-Vaquero, et al.
Scientific Reports|February 17, 2026
Predicting multiphase flow and tracer transport for an underground chemical explosive testJohn P Ortiz, Dolan D Lucero, Esteban Rougier, et al.
CHEST Critical Care|December 15, 2025
Epidemiologic Characteristics and Management of Sepsis Among Previously Healthy PatientsRachel K Hechtman, Megan E Heath, Jennifer K Horowitz, et al.
Pageof 44

Showing results (371-380 of 431) with videos related to

Sort By:
Pageof 44
Blood Cancer Discovery|January 12, 2022
Genetic and Transcriptional Contributions to Relapse in Normal Karyotype Acute Myeloid LeukemiaAllegra A Petti, Saad M Khan, Ziheng Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short statureAlfonso Hisado-Oliva, Alba Ruzafa-Martin, Lucia Sentchordi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 21, 2017
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone TherapyGabriela A Vasques, Mariana F A Funari, Frederico M Ferreira, et al.
Clinical Genetics|April 30, 2023
Evolution of clinical and radiological presentations of spondyloepimetaphyseal dysplasia, RPL13-related: Description of 11 further casesFrancisca Díaz-González, Manuel Parrón-Pajares, Elsa Lucas-Castro, et al.
Journal of Hematology & Oncology|February 19, 2013
A double-blind, randomized, multicenter phase 2 study of prasugrel versus placebo in adult patients with sickle cell diseaseTed Wun, Denis Soulieres, Andrew L Frelinger, et al.
American Journal of Human Genetics|September 22, 2005
A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosisSara Benito-Sanz, N Simon Thomas, Céline Huber, et al.
Journal of Medical Genetics|October 27, 2020
Biallelic cGMP-dependent type II protein kinase gene (<i>PRKG2</i>) variants cause a novel acromesomelic dysplasiaFrancisca Díaz-González, Saruchi Wadhwa, Maria Rodriguez-Zabala, et al.
Revista Espanola De Cardiologia (English Ed.)|November 18, 2017
In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular PhenotypeLuis Fernández, Jair Tenorio, Coral Polo-Vaquero, et al.
Scientific Reports|February 17, 2026
Predicting multiphase flow and tracer transport for an underground chemical explosive testJohn P Ortiz, Dolan D Lucero, Esteban Rougier, et al.
CHEST Critical Care|December 15, 2025
Epidemiologic Characteristics and Management of Sepsis Among Previously Healthy PatientsRachel K Hechtman, Megan E Heath, Jennifer K Horowitz, et al.
Pageof 44