Ria Garg
3PUBLICATIONS
2CO-AUTHORS
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Publications (3)
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|Sep 16, 2025
Evidence of maternal inheritance of Nizon-Isidor syndrome in an individual with GAMT and TNFRSF13B sequence variants.Dibyendu Dutta, Jennifer Black, Daniela Macaya
|Aug 04, 2025
Chromosome 1p31.1 Deletion: A Case With Developmental Delay, Hypotonia, Cryptorchidism, Abnormal Oral Frenulum, and Feet Deformity.Tatiana Mikhailova, Ria Garg
|Nov 06, 2023
KCNK4-related channelopathy causing a neurodevelopmental syndrome.Ria Garg, Joseph Sullivan, David Blair
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