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

द्वारा Lall, Meena, Puri, Ratna, Saviour, Pushpa, Verma, Ishwar
प्रकाशित 2012

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

द्वारा Kalotra, Vishali, Lall, Meena, Saviour, Pushpa, Verma, Ishwar Chander, Kaur, Anupam
में प्रकाशित J Hum Reprod Sci (2017)

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

द्वारा Lall, Meena, Saviour, Pushpa, Puri, Ratna, Paliwal, Preeti, Mahajan, Surbhi, Verma, Ishwar
प्रकाशित 2014

Allelic variants of DYX1C1 are not associated with dyslexia in India

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

Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience

द्वारा Bajaj Lall, Meena, Agarwal, Shruti, Paliwal, Preeti, Saviour, Pushpa, Joshi, Anju, Joshi, Arti, Mahajan, Surbhi, Bijarnia-Mahay, Sunita, Dua Puri, Ratna, Verma, I. C.
में प्रकाशित J Obstet Gynaecol India (2021)