[1]
Haleema, N., Anjum, B. and Begum, S. 2024. Immunodeficiency, centromeric instability and facial anomalies syndrome type 1-homozygous c.2301+2_2301+24del mutation in DNMT3B gene. International Journal of Contemporary Pediatrics. 11, 11 (Oct. 2024), 1651–1653. DOI:https://doi.org/10.18203/2349-3291.ijcp20243094.