Alyce V. Belonis

Medical Genetics | Pediatrics | Psychiatry

705 Riley Hospital Dr
Indianapolis, IN 46202

Last Updated: 09/26/2026

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Found 6 publications

Genetics 101: When to Refer.

Genetics 101: When to Refer.

Journal: Pediatric clinics of North America

Published: September 13, 2023

Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individuals.

Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individuals.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 26, 2023

Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center.

Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center.

Journal: Frontiers in genetics

Published: March 01, 2022

Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.

Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.

Journal: Clinical case reports

Published: October 07, 2021

Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz Syndrome.

Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz Syndrome.

Journal: Pediatric cardiology

Published: November 30, 2020

An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3.

An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3.

Journal: American journal of medical genetics. Part A

Published: May 01, 2019

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Last Updated: 09/26/2026