A novel mutation in the MECOM gene causing radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT-2) in an infant.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Works by Thangadorai, Ravikumar
Results: 4
1
2
Targeted Next Generation Sequencing (NGS) to Diagnose Hereditary Hemolytic Anemias.
- Published in:
- International Journal of Hematology-Oncology & Stem Cell Research, 2020, v. 14, n. 3, p. 177
- By:
- Publication type:
- Article
3
Primary Pulmonary Diffuse Large B-Cell Non-Hodgkin's Lymphoma in a Child.
- Published in:
- Indian Journal of Chest Diseases & Allied Sciences, 2013, v. 55, n. 4, p. 225
- By:
- Publication type:
- Article
4
Clinical Profile of Febrile Neutropenia in Children with Malignancies in a Tertiary Care Hospital: A Prospective Observational Study.
- Published in:
- Indian Journal of Medical & Paediatric Oncology, 2025, v. 46, n. 1, p. 77, doi. 10.1055/s-0044-1788702
- By:
- Publication type:
- Article