APA (7th ed.) Citation

Shah, J., Mondal, D., Jain, D., Mhatre, P., Patel, K., Iyer, A., . . . Sheth, H. (2025). Long read whole genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic autism spectrum disorder in India. BMC Medical Genomics, 18(1), 1. https://doi.org/10.1186/s12920-025-02204-6

Chicago Style (17th ed.) Citation

Shah, Jhanvi, et al. "Long Read Whole Genome Sequencing-based Discovery of Structural Variants and Their Role in Aetiology of Non-syndromic Autism Spectrum Disorder in India." BMC Medical Genomics 18, no. 1 (2025): 1. https://doi.org/10.1186/s12920-025-02204-6.

MLA (9th ed.) Citation

Shah, Jhanvi, et al. "Long Read Whole Genome Sequencing-based Discovery of Structural Variants and Their Role in Aetiology of Non-syndromic Autism Spectrum Disorder in India." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 1, https://doi.org/10.1186/s12920-025-02204-6.