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

Por Lall, Meena, Puri, Ratna, Saviour, Pushpa, Verma, Ishwar
Publicado em 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 no J Hum Reprod Sci (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 em 2011

A Bi-Lineal Acute Leukemia (T/Myeloid, NOS) with Complex Cytogenetic Abnormalities

Por Sharma, Prashant, Lall, Meena, Jain, Paresh, Saraf, Amrita, Sachdeva, Anupam, Bhargava, Manorama
Publicado em 2012

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 em 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 no J Hum Reprod Sci (2016)

Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p

Por Sharma, Pankaj, Gupta, Neerja, Chowdhury, Madhumita R., Sapra, Savita, Shukla, Rashmi, Lall, Meena, Kabra, Madhulika
Publicado no J Pediatr Genet (2013)