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

A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum

por Lall, Meena, Thakur, Seema, Puri, Ratna, Verma, Ishwar, Mukerji, Mithali, Jha , Pankaj
Publicado 2011

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

Preimplantation genetic screening for all 24 chromosomes by microarray comparative genomic hybridization significantly increases implantation rates and clinical pregnancy rates in...

por Majumdar, Gaurav, Majumdar, Abha, Lall, Meena, Verma, Ishwar C., Upadhyaya, Kailash C.
Publicado 2016

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