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Elizabeth Sellars

Showing results (1-10 of 6) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2015
Aortic dilation, genetic testing, and associated diagnosesYuri A Zarate, Elizabeth Sellars, Tiffany Lepard, et al.
European Journal of Pediatrics|June 14, 2015
Aortic dilation in pediatric patientsYuri A Zarate, Elizabeth Sellars, Tiffany Lepard, et al.
American Journal of Medical Genetics. Part A|May 22, 2014
Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literatureYuri A Zarate, Tiffany Lepard, Elizabeth Sellars, et al.
Journal of Personalized Medicine|June 2, 2021
Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children's HospitalPritmohinder S Gill, Feliciano B Yu, Patricia A Porter-Gill, et al.
Human Molecular Genetics|October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophyYanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2015
Aortic dilation, genetic testing, and associated diagnosesYuri A Zarate, Elizabeth Sellars, Tiffany Lepard, et al.
European Journal of Pediatrics|June 14, 2015
Aortic dilation in pediatric patientsYuri A Zarate, Elizabeth Sellars, Tiffany Lepard, et al.
American Journal of Medical Genetics. Part A|May 22, 2014
Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literatureYuri A Zarate, Tiffany Lepard, Elizabeth Sellars, et al.
Journal of Personalized Medicine|June 2, 2021
Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children's HospitalPritmohinder S Gill, Feliciano B Yu, Patricia A Porter-Gill, et al.
Human Molecular Genetics|October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophyYanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.
Science Advances|December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Dong Li, Samuel G Cox, et al.
Pageof 1