Cytogenetics of fragile X Chromosome: Frequency association and their implications in subjects with autism
systematic and comparitive study on the association and significance of chromosomal aberrations in subjects with idiopathic mental retardation, cogenital malformations and syndromes
Comprehensive genetic investigation into the aetiology of isolated polymicrogyria
Investigation of cytogenetic and molecular genetics variants interwined with recurrent pregnancy loss(RPL)
Comprehensive investigation into focal malformations of cortical development by ultra deep sequencing and deep phenotyping in drug resistant epilepsy
