• https://doi.org/10.1186/s12920-020-00796-9, Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report

  • A rare case of a male child with post-zygotic de novo mosaic variant c.538C>T in MECP2 gene: a case report of Rett syndrome

    https://bmcneurol.biomedcentral.com/articles/10.1186/s12883-021-02500-5. (n.d.).

  • Volume 62, Issue S4- Special Issue: Abstracts of the 32nd Annual Meeting of the European Academy of Childhood Disability (EACD) – Virtual Meeting, 25–28 November 2020 (page no 34-35), https://doi.org/10.1111/dmcn.14688.

  • British Paediatric Neurology Association. Abstracts of the Annual Meeting, 6-8 January 2021, Virtual. Developmental Medicine & Child Neurology. 2021; 63 (S1)

  • https://onlinelibrary.wiley.com/toc/14698749/2022/64/S1- page 41, Poster presented in BPNA “British Paediatric Neurology Association” annual meeting held in Jan 2022.