Varuna Chander
0000-0003-2610-9381
3 papers found
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Long read sequencing and expression studies of AHDC1 deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism
Long read sequencing and expression studies ofAHDC1deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism
Evaluation of computational genotyping of structural variation for clinical diagnoses
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