Publications by authors named "Meena Lall"

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Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of 300 Indian Patients.
Meena Bajaj Lall, Anju Joshi, Shruti Agarwal, Pushpa Saviour, Preeti Paliwal

Indian J Pediatr· January 2026

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Translocation t(X;Y) characterized by chromosomal microarray and FISH in a phenotypic male with Microphthalmia and linear skin defects.
Kanika Singh, Meena Lall, Shruti Agarwal, Ratna D Puri

Clin Dysmorphol· January 2024

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A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia.
Luna Bajracharya, Meena Lall, Sunita Bijarnia-Mahay, Praveen Kumar, Imran Mushtaq

Case Rep Genet· October 2023

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Hypomelanosis of Ito.
Veronika Arora, Rinky Tandon, Ratna Dua Puri, Meena Lall, Imran Noorani

Indian J Pediatr· November 2022

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Prenatal phenotypic spectrum of full trisomy 18 in an Indian cohort.
Sapna Sandal, Sunita Bijarnia Mahay, Nandita Dimri Gupta, Renu Saxena, Meena Lall

Am J Med Genet A· June 2022

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Clinical and Genetic Profile of Children With Short Stature Presenting to a Genetic Clinic in Northern India.
Kanika Singh, Ratna Dua Puri, Sunita Bijarnia-Mahay, Meena Lall, Jyotsna Verma

Indian Pediatr· June 2022

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Study of Cytogenetic Alterations and Association With Prognostic Factors in Indian Children With B-Lineage Acute Lymphoblastic Leukemia.
Manisha Agarwal, Rachna Seth, Meena Lall

Clin Lymphoma Myeloma Leuk· July 2020

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Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent hybridization.
Venkataswamy Eswarachari, Priya Kadam, Sireesha Movva, Shruthi Lingaiah, Riyaz M Akther, Meena Lall

J Matern Fetal Neonatal Med· December 2019

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Extending the Phenotype and Identification of a Novel Candidate Gene for Immunodeficiency in 5q11 Microdeletion Syndrome.
Veronica Arora, Shruti Aggarwal, Sunita Bijarnia, Meena Lall, Anju Joshi

Mol Syndromol· January 2019

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Fetal valproate syndrome as a phenocopy of Kleefstra syndrome.
Veronica Arora, Anju Joshi, Meena Lall, Shruti Agarwal, Sunita Bijarnia Mahay

Birth Defects Res· September 2018

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Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case-control Study.
Vishali Kalotra, Meena Lall, Pushpa Saviour, Ishwar Chander Verma, Anupam Kaur

J Hum Reprod Sci· January 2017

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Is the diagnostic yield influenced by the indication for fetal autopsy?
Ratna Dua Puri, Udhaya Kotecha, Meena Lall, Pratima Dash, Sunita Bijarnia-Mahay

Am J Med Genet A· August 2016

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Preimplantation genetic screening for all 24 chromosomes by microarray comparative genomic hybridization significantly increases implantation rates and clinical pregnancy rates in patients undergoing in vitro fertilization with poor prognosis.
Gaurav Majumdar, Abha Majumdar, Meena Lall, Ishwar C Verma, Kailash C Upadhyaya

J Hum Reprod Sci· July 2016

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Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p.
Pankaj Sharma, Neerja Gupta, Madhumita R Chowdhury, Savita Sapra, Rashmi Shukla, Meena Lall

J Pediatr Genet· September 2013

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A Bi-Lineal Acute Leukemia (T/Myeloid, NOS) with Complex Cytogenetic Abnormalities.
Prashant Sharma, Meena Lall, Paresh Jain, Amrita Saraf, Anupam Sachdeva

Indian J Hematol Blood Transfus· June 2013

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Down syndrome in India--diagnosis, screening, and prenatal diagnosis.
Ishwar C Verma, Meena Lall, Ratna Dua Puri

Clin Lab Med· June 2012

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Childhood acute lymphoblastic leukemia outcome in India: progress on all fronts.
Satya Prakash Yadav, Mohammed Ramzan, Meena Lall, Anupam Sachdeva

J Pediatr Hematol Oncol· May 2012

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A familial deletion 4q syndrome: An outcome of a paracentric inversion.
Meena Lall, Ratna Puri, Pushpa Saviour, Ishwar Verma

Indian J Hum Genet· May 2012

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Pediatric acute myeloid leukemia: final frontier for pediatric oncologists in developing world.
Satya Prakash Yadav, Mohammed Ramzan, Meena Lall, Anupam Sachdeva

Pediatr Hematol Oncol· November 2011

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A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum.
Meena Lall, Seema Thakur, Ratna Puri, Ishwar Verma, Mithali Mukerji

Mol Cytogenet· September 2011

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Genetic counseling and prenatal diagnosis in India--experience at Sir Ganga Ram Hospital.
I C Verma, Renu Saxena, Meena Lall, Sunita Bijarnia, Rajesh Sharma

Indian J Pediatr· April 2003

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