Genetic counseling and prenatal diagnosis in India—experience at Sir Ganga Ram Hospital IC Verma, R Saxena, M Lall, S Bijarnia, R Sharma The Indian Journal of Pediatrics 70, 293-297, 2003 | 50 | 2003 |
The HLA‐G 14 bp insertion/deletion polymorphism and its association with soluble HLA‐G levels in women with recurrent miscarriages V Kalotra, M Lall, IC Verma, A Kaur, A Kaur Hla 91 (3), 167-174, 2018 | 26 | 2018 |
Down syndrome in India—diagnosis, screening, and prenatal diagnosis IC Verma, M Lall, RD Puri Clinics in laboratory medicine 32 (2), 231-248, 2012 | 20 | 2012 |
Childhood acute lymphoblastic leukemia outcome in India: progress on all fronts SP Yadav, M Ramzan, M Lall, A Sachdeva Journal of Pediatric Hematology/Oncology 34 (4), 324, 2012 | 18 | 2012 |
Pediatric acute myeloid leukemia: final frontier for pediatric oncologists in developing world SP Yadav, M Ramzan, M Lall, A Sachdeva Pediatric Hematology and Oncology 28 (8), 647-648, 2011 | 18 | 2011 |
The changing scenario in prenatal diagnosis of genetic disorders: genetics to genomics S Bijarnia-Mahay, V Arora, RD Puri, M Lall, R Saxena, J Verma, A Baijal, ... Current Medicine Research and Practice 8 (6), 203-208, 2018 | 15 | 2018 |
Using noninvasive prenatal testing for aneuploidies in a developing country: lessons learnt P Dash, RD Puri, U Kotecha, S Bijarnia, M Lall, IC Verma Journal of Fetal Medicine 1 (03), 131-135, 2014 | 15 | 2014 |
Preimplantation genetic screening for all 24 chromosomes by microarray comparative genomic hybridization significantly increases implantation rates and clinical pregnancy rates … G Majumdar, A Majumdar, M Lall, IC Verma, KC Upadhyaya Journal of human reproductive sciences 9 (2), 94-100, 2016 | 14 | 2016 |
A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum M Lall, S Thakur, R Puri, I Verma, M Mukerji, P Jha Molecular Cytogenetics 4, 1-9, 2011 | 14 | 2011 |
Prevalence of cytogenetic anomalies in couples with recurrent miscarriages: A case–control study V Kalotra, M Lall, P Saviour, IC Verma, A Kaur Journal of human reproductive sciences 10 (4), 302-309, 2017 | 13 | 2017 |
FISH is not suitable as a standalone test for detecting fetal chromosomal abnormalities M Lall, S Mahajan, P Saviour, P Paliwal, A Joshi, N Setia, IC Verma Journal of Fetal Medicine 2 (02), 53-59, 2015 | 11 | 2015 |
Prenatal diagnosis by chromosome microarray analysis, an Indian experience M Bajaj Lall, S Agarwal, P Paliwal, P Saviour, A Joshi, A Joshi, S Mahajan, ... The Journal of Obstetrics and Gynecology of India 71, 156-167, 2021 | 7 | 2021 |
Is the diagnostic yield influenced by the indication for fetal autopsy? RD Puri, U Kotecha, M Lall, P Dash, S Bijarnia‐Mahay, IC Verma American Journal of Medical Genetics Part A 170 (8), 2119-2126, 2016 | 6 | 2016 |
Absent/hypoplastic fetal nasal bone and its association with aneuploidies P Dash, RD Puri, M Goyal, S Bijarnia, M Lall, U Kotecha, IC Verma Journal of fetal medicine 2, 75-78, 2015 | 6 | 2015 |
Outcome of Prenatally-Detected Fetal Ventriculomegaly ICV Sunita Bijarnia-Mahay, Ratna D. Puri,Udhaya Kotecha,Pratima Dash,Swasti ... J Fetal Med 2, 39–44, 2015 | 6 | 2015 |
Need for fetal autopsy and genetic diagnosis in fetal limb anomalies UH Kotecha, RD Puri, P Dash, S Bijarnia-Mahay, M Lall, IC Verma Journal of Fetal Medicine 1 (03), 151-157, 2014 | 6 | 2014 |
Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p.Case Report. MK P Sharma, N Gupta, M Roy, S Sapra, R Shukla, M Lall Journal of Pediatric Genetics 2, 163-169, 2013 | 5 | 2013 |
A familial deletion 4q syndrome: An outcome of a paracentric inversion M Lall, R Puri, P Saviour, I Verma Indian Journal of Human Genetics 18 (2), 238, 2012 | 5 | 2012 |
Hypomelanosis of Ito V Arora, R Tandon, RD Puri, M Lall, I Noorani, P Suman Indian Journal of Pediatrics 89 (11), 1117-1119, 2022 | 4 | 2022 |
Fetal valproate syndrome as a phenocopy of Kleefstra syndrome V Arora, A Joshi, M Lall, S Agarwal, S Bijarnia Mahay, R Dua puri, ... Birth Defects Research 110 (15), 1205-1209, 2018 | 4 | 2018 |