Unlocking the genetic blueprint of duchenne muscular dystrophy: A personalized approach with MLPA and WES.
- Published in:
- Global Medical Genetics, 2025, v. 12, n. 2, p. 1, doi. 10.1016/j.gmg.2025.100038
- By:
- Publication type:
- Article
Works matching AU Mathur, Priyanshu
Results: 6
1
2
Limb-Girdle Muscular Dystrophies (LGMD): Clinical features, diagnosis and genetic variability through next generation sequencing.
- Published in:
- Global Medical Genetics, 2025, v. 12, n. 1, p. 1, doi. 10.1016/j.gmg.2024.100035
- By:
- Publication type:
- Article
3
A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing Impairment.
- Published in:
- Indian Journal of Otolaryngology & Head & Neck Surgery, 2023, v. 75, n. 4, p. 3575, doi. 10.1007/s12070-023-03948-2
- By:
- Publication type:
- Article
4
Antiviral Therapy in Cytomegalovirus-Associated Biliary Atresia.
- Published in:
- 2022
- By:
- Publication type:
- Letter
5
Cholestatic Jaundice and Cytomegalovirus Infection in Children – An Observational Study.
- Published in:
- Chrismed: Journal of Health & Research, 2024, v. 11, n. 3, p. 134, doi. 10.4103/cjhr.cjhr_117_23
- By:
- Publication type:
- Article
6
Fetal Valproate Syndrome with Limb Defects: An Indian Case Report.
- Published in:
- 2016
- By:
- Publication type:
- Case Study