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Meena Bajaj Lall
Meena Bajaj Lall
Senior Consultant, Head Cytogenetics Laboratory, Institute of Medical Genetics and Genomics, Sir
在 sgrh.com 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
502003
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
262018
Down syndrome in India—diagnosis, screening, and prenatal diagnosis
IC Verma, M Lall, RD Puri
Clinics in laboratory medicine 32 (2), 231-248, 2012
202012
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
182012
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
182011
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
152018
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
152014
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
142016
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
142011
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
132017
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
112015
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
72021
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
62016
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
62015
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
62015
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
62014
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
52013
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
52012
Hypomelanosis of Ito
V Arora, R Tandon, RD Puri, M Lall, I Noorani, P Suman
Indian Journal of Pediatrics 89 (11), 1117-1119, 2022
42022
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
42018
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