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Repeated pregnancy losses with multiple aneuploidies and major genomic imbalance: A case report

Asian pacific journal of reproduction, 2024-05, Vol.13 (3), p.143-146

2024

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Transformation to telephonic genetic counselling during SARS-CoV-2 pandemic: challenges and suggested protocol in Indian scenario

Journal of genetics, 2022-06, Vol.101 (1), Article 28

2022

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A retrospective analysis of COVID-19 diagnosis results obtained by rapid antigen tests and RT-PCR: Implications for disease management

Indian journal of medical microbiology, 2021-10, Vol.39 (4), p.537-539

2021

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Detection of SARS-CoV-2 infection by RT-PCR test: factors influencing interpretation of results

Virusdisease, 2021-06, Vol.32 (2), p.187-189

2021

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Severe acute respiratory syndrome coronavirus 2 positivity in neonates born to coronavirus disease 2019-positive mothers: A retrospective data analysis

Indian journal of public health, 2023-04, Vol.67 (2), p.333-334

2023

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A Novel Methyl-CpG Binding Protein 2 (MECP2) Variant in an Indian Girl with Rett Syndrome

Journal of clinical and diagnostic research, 2021-04, Vol.15 (4), p.GD04-GD06

2021

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Spectrum of germline BRCA mutations in hereditary breast and ovarian cancer syndrome in Indian population: A central reference laboratory experience

Cancer Research, Statistics, and Treatment, 2020-01, Vol.3 (1), p.32-41

2020

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Elevated Risk of COVID-19 Infection among People Living with HIV in Mumbai—A Retrospective Study

Re:GEN open, 2022-01, Vol.2 (1), p.72-74

2022

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Exome Sequencing, whom to Test? A Case Report of Rare Genetic Findings in Consanguineous Couple with Two Neonatal Deaths

Journal of obstetrics and gynaecology of India, 2022-12, Vol.72 (Suppl 2), p.409-411

2022

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Evaluation of Single Exon Deletions in DMD/BMD: Technical and Analytical Concerns

Neurology India, 2022-07, Vol.70 (4), p.1615-1617

2022

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Two Novel Variants Associated with Brain Abnormalities in Clinical Suspicion of Arthrogryposis and Similar Phenotype in Three Children: Challenges in Offering Prenatal Diagnosis

Journal of obstetrics and gynaecology of India, 2024-06, Vol.74 (3), p.271-274

2024

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Emphasizing the need for preconceptional, prenatal genetic counseling and comprehensive genetic testing in consanguinity: challenges and experience

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.91, Article 91

2024

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A complex karyotype with t

Indian journal of cancer, 2020-07, Vol.57 (3), p.330

2020

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A complex karyotype with t(11;12)(q23;p13) translocation with coexistent clones of deletion 5q and cryptic deletion 7q in acute myeloid leukemia

Indian journal of cancer, 2020-07, Vol.57 (3), p.330-333

2020

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Relevance of augmented kisspeptin signaling through H364 KISS1R in central precocious puberty

Gene, 2024-02, Vol.895, p.148016-148016, Article 148016

2024

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The dynamics of SARS-CoV-2 infection in unvaccinated and vaccinated populations in Mumbai, India, between 28 December 2020 and 30 August 2021

Archives of virology, 2023-07, Vol.168 (7), p.188-188, Article 188

2023

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A novel CFTR gene variant - p.Tyr517 associated with cystic fibrosis: a case report

Fetal and pediatric pathology, 2018-12, Vol.37 (6), p.448-451

2018

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Cytomegalovirus reactivation in a SARS-CoV-2 infected woman experiencing fetal demise in the first trimester with fetal trisomy 21: A case report

Indian journal of medical microbiology, 2023-01, Vol.41, p.1-4

2023

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An Approach to Resolve Uncertainty in COVID-19 Diagnosis due to Inconclusive Results from RT-PCR Test

Journal of the Association of Physicians of India, 2022-06, Vol.70 (6), p.11-12

2022

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A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington’s Disease Symptoms

Molecular diagnosis & therapy, 2018-06, Vol.22 (3), p.353-359

2018

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Relevance of augmented kisspeptin signaling through H 364 KISS1R in central precocious puberty

Gene, 2024-02, Vol.895, p.148016

2024

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Frequency of Chromosomal Abnormalities in Products of Conception: A Retrospective, Large-scale, Single-center study

Journal of SAFOG (South Asian Federation of Obstetrics and Gynecology), 2019-12, Vol.11 (6), p.381-384

2019

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Acute Myeloid Leukemia with complex hyperdiploidkaryotypeA Case Report

Annals of pathology and laboratory medicine, 2018-12, Vol.2 (12), p.C185-189

2018

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Frequency of down syndrome: an experience of a tertiary care diagnostic laboratory in India

International Journal of Advances in Medicine, 2017-11, Vol.4 (6), p.1672

2017

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Cytogenetics and Importance of Genetic Counselling in Recurrent Pregnancy Losses: Experience from Tertiary Care Laboratory

IRA-International Journal of Applied Sciences (ISSN 2455-4499), 2017-10, Vol.9 (1), p.9

2017

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Repeated pregnancy losses with multiple aneuploidies and major genomic imbalance: A case report

Transformation to telephonic genetic counselling during SARS-CoV-2 pandemic: challenges and suggested protocol in Indian scenario

A retrospective analysis of COVID-19 diagnosis results obtained by rapid antigen tests and RT-PCR: Implications for disease management

Detection of SARS-CoV-2 infection by RT-PCR test: factors influencing interpretation of results

Severe acute respiratory syndrome coronavirus 2 positivity in neonates born to coronavirus disease 2019-positive mothers: A retrospective data analysis

A Novel Methyl-CpG Binding Protein 2 (MECP2) Variant in an Indian Girl with Rett Syndrome

Spectrum of germline BRCA mutations in hereditary breast and ovarian cancer syndrome in Indian population: A central reference laboratory experience

Elevated Risk of COVID-19 Infection among People Living with HIV in Mumbai—A Retrospective Study

Exome Sequencing, whom to Test? A Case Report of Rare Genetic Findings in Consanguineous Couple with Two Neonatal Deaths

Evaluation of Single Exon Deletions in DMD/BMD: Technical and Analytical Concerns

Two Novel Variants Associated with Brain Abnormalities in Clinical Suspicion of Arthrogryposis and Similar Phenotype in Three Children: Challenges in Offering Prenatal Diagnosis

Emphasizing the need for preconceptional, prenatal genetic counseling and comprehensive genetic testing in consanguinity: challenges and experience

A complex karyotype with t

A complex karyotype with t(11;12)(q23;p13) translocation with coexistent clones of deletion 5q and cryptic deletion 7q in acute myeloid leukemia

Relevance of augmented kisspeptin signaling through H364 KISS1R in central precocious puberty

The dynamics of SARS-CoV-2 infection in unvaccinated and vaccinated populations in Mumbai, India, between 28 December 2020 and 30 August 2021

A novel CFTR gene variant - p.Tyr517 associated with cystic fibrosis: a case report

Cytomegalovirus reactivation in a SARS-CoV-2 infected woman experiencing fetal demise in the first trimester with fetal trisomy 21: A case report

An Approach to Resolve Uncertainty in COVID-19 Diagnosis due to Inconclusive Results from RT-PCR Test

A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington’s Disease Symptoms

Relevance of augmented kisspeptin signaling through H 364 KISS1R in central precocious puberty

Frequency of Chromosomal Abnormalities in Products of Conception: A Retrospective, Large-scale, Single-center study

Acute Myeloid Leukemia with complex hyperdiploidkaryotypeA Case Report

Frequency of down syndrome: an experience of a tertiary care diagnostic laboratory in India

Cytogenetics and Importance of Genetic Counselling in Recurrent Pregnancy Losses: Experience from Tertiary Care Laboratory

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