A familial deletion 4q syndrome: An outcome of a paracentric inversion

por Lall, Meena, Puri, Ratna, Saviour, Pushpa, Verma, Ishwar
Publicado 2012

Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case–control Study

por Kalotra, Vishali, Lall, Meena, Saviour, Pushpa, Verma, Ishwar Chander, Kaur, Anupam
Publicado 2017

Combined classical cytogenetics and array Comparative Genomic Hybridisation for genomic copy number analysis

por Lall, Meena, Saviour, Pushpa, Puri, Ratna, Paliwal, Preeti, Mahajan, Surbhi, Verma, Ishwar
Publicado 2014

Allelic variants of DYX1C1 are not associated with dyslexia in India

por Saviour, Pushpa, Kumar, Satish, Kiran, U., Ravuri, Rajasekhara Reddy, Rao, V. R., Ramachandra, Nallur Basappa
Publicado 2008

A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia

por Bajracharya, Luna, Lall, Meena, Bijarnia-Mahay, Sunita, Kumar, Praveen, Mushtaq, Imran, Saviour, Pushpa, Paliwal, Preeti, Joshi, Anju, Agarwal, Shruti, Suman, Praveen
Publicado 2023