eP318: Concurrent somatic 9p21 deletion and germline EP300 variant in a patient with T-ALL, immunodeficiency and malformations: Phenotypic expansion or comorbidities?
Authors:
- Subit BaruaSBSubit Barua
- Theresa KowalskiTKTheresa Kowalski
- Vundavalli MurtyVMVundavalli Murty
- Alejandro IglesiasAIAlejandro Iglesias
- Jun LiaoJLJun Liao
- 21 March 2022
- journal article
- abstracts
- Published by Elsevier in Genetics in Medicine
- Vol. 24 (3) , S199-S200