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Stephanie M Ware

Showing results (141-150 of 147) with videos related to

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American Journal of Respiratory and Critical Care Medicine|June 16, 2018
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice GuidelineAdam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
Journal of the American Heart Association|April 28, 2021
Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes StudyStephanie M Ware, James D Wilkinson, Muhammad Tariq, et al.
European Journal of Human Genetics : EJHG|September 6, 2023
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous returnEmily A Huth, Xiaonan Zhao, Nichole Owen, et al.
Cell Reports. Medicine|March 4, 2022
Genetic resiliency associated with dominant lethal <i>TPM1</i> mutation causing atrial septal defect with high heritabilityPolakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.
American Journal of Medical Genetics. Part A|March 10, 2022
The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discoveryMaria I Kontaridis, Amy E Roberts, Lisa Schill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2023
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Pageof 15

Showing results (141-150 of 147) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 147 results.
American Journal of Respiratory and Critical Care Medicine|June 16, 2018
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice GuidelineAdam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
Journal of the American Heart Association|April 28, 2021
Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes StudyStephanie M Ware, James D Wilkinson, Muhammad Tariq, et al.
European Journal of Human Genetics : EJHG|September 6, 2023
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous returnEmily A Huth, Xiaonan Zhao, Nichole Owen, et al.
Cell Reports. Medicine|March 4, 2022
Genetic resiliency associated with dominant lethal <i>TPM1</i> mutation causing atrial septal defect with high heritabilityPolakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.
American Journal of Medical Genetics. Part A|March 10, 2022
The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discoveryMaria I Kontaridis, Amy E Roberts, Lisa Schill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 2, 2023
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded proteinElke de Boer, Charlotte W Ockeloen, Rosalie A Kampen, et al.
Pageof 15