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Alyce Belonis

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

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Pediatric Clinics of North America|September 13, 2023
Genetics 101: When to ReferAlyce Belonis, Sofia Saenz Ayala
Clinical Case Reports|February 14, 2022
Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case reportSubba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini, et al.
Pediatric Cardiology|April 13, 2021
Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz SyndromeShannon K Powell, Hassan Almeneisi, Tarek Alsaied, et al.
Frontiers in Genetics|August 8, 2022
Clinically available testing options resulting in diagnosis in post-exome clinic at one medical centerElizabeth K Baker, Elizabeth A Ulm, Alyce Belonis, et al.
American Journal of Medical Genetics. Part A|September 13, 2019
An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3Valerie J Castelluccio, Francesco Vetrini, Ty Lynnes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2023
Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individualsQuentin Sabbagh, Sadegheh Haghshenas, Juliette Piard, et al.
Pageof 1

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

Sort By:
Pageof 1
Pediatric Clinics of North America|September 13, 2023
Genetics 101: When to ReferAlyce Belonis, Sofia Saenz Ayala
Clinical Case Reports|February 14, 2022
Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case reportSubba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini, et al.
Pediatric Cardiology|April 13, 2021
Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz SyndromeShannon K Powell, Hassan Almeneisi, Tarek Alsaied, et al.
Frontiers in Genetics|August 8, 2022
Clinically available testing options resulting in diagnosis in post-exome clinic at one medical centerElizabeth K Baker, Elizabeth A Ulm, Alyce Belonis, et al.
American Journal of Medical Genetics. Part A|September 13, 2019
An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3Valerie J Castelluccio, Francesco Vetrini, Ty Lynnes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2023
Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individualsQuentin Sabbagh, Sadegheh Haghshenas, Juliette Piard, et al.
Pageof 1