Detection of 22q11.2 deletion syndrome by single-nucleotide polymorphism based non-invasive prenatal test
Angela Devanboo*, Dhriti Chendil Nathan, Shweta Kannan Mahalingam, Vishalakshi Apparaya Prabhu, Hema Purandarey, E Venkataswamy, V. L. Ramprasad, Priya Kadam