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Updated: Jun 25, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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A new case of SUPT16H-associated syndromic neurodevelopmental delay

Surya Balakrishnan1, Mouneesha Rachamadugu, Aneek Das Bhowmik

  • 1Molecular Diagnostic division, Center for Cellular and Molecular Biology [CCMB], Uppal, Hyderabad, India.

Clinical Dysmorphology
|May 31, 2024
PubMed
Abstract

No abstract available in PubMed .

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