Gandham SriLakshmi Bhavani

5PUBLICATIONS
10CO-AUTHORS
Analytical spectrometryNeonatologyNeurogeneticsAdolescent healthMedical bacteriology
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Publications (5)

|Oct 25, 2023
Indian patients with CHST3-related chondrodysplasia with congenital joint dislocations.

Swati Singh, Prince Jacob, Siddaramappa J Patil

|Feb 11, 2023
Nuclear Mitochondrial Disorder Due to a Variant in NAXE in Two Unrelated Indian Children.

Swathi Sunil Rao, Gandham Srilakshmi Bhavani, Anil B Jalan

|Dec 16, 2022
Genome sequencing identifies a large non-coding region deletion of SNX10 causing autosomal recessive osteopetrosis.

Prajna Udupa, Debasish Kumar Ghosh, Neethukrishna Kausthubham

|Nov 09, 2021
Pseudoachondroplasia: Phenotype and genotype in 11 Indian patients.

Prince Jacob, Gandham Sri Lakshmi Bhavani, Hitesh Shah

|Mar 19, 2020
Burn-McKeown syndrome with biallelic promoter type 2 deletion in TXNL4A in two siblings.

Dhanya L Narayanan, Greeshma Purushothama, Gandham Sl Bhavani

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