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A Case of Partial Trisomy of 10q and Partial Monosomy of 6p Resulting from Maternal t(6;10) (p23;q24)

Journal of clinical and diagnostic research, 2021-08, Vol.15 (8), p.GD01-GD03

2021

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Atypical Co-amplification with Co-localization of HER2 Gene in Breast Cancer: Combined IHC/FISH Approach as per ASCO/CAP 2018 Guidelines for Targeted Therapy Eligibility

Indian journal of surgical oncology, 2024-03, Vol.15 (1), p.8-11

2024

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Atypical MYC rearrangement pattern of 3′ deletion and 5′ amplification along with independent IGH rearrangement: A case study

Indian journal of cancer, 2022-10, Vol.59 (4), p.548-551

2022

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Derivative 6 as an additional chromosomal abnormality along with t(15;17): A case report

Indian journal of cancer, 2022-07, Vol.59 (3), p.419-421

2022

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Tetrasomy 8 in Haematological Malignancies-A Case Series

Journal of clinical and diagnostic research, 2021-09, Vol.15 (9), p.GR01-GR03

2021

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Pentasomy X Syndrome in Neonate: A Rare Disorder

Journal of clinical and diagnostic research, 2021-04, Vol.15 (4), p.GD01-GD03

2021

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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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Derivative 6 as an additional chromosomal abnormality along with t

Indian journal of cancer, 2022-07, Vol.59 (3), p.419

2022

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A novel coexistence of tetrasomy 8 and FLT3-ITD along with variant 3 way translocation t(4;17;15) in acute promyelocytic leukemia: Case study and literature review

Cancer genetics, 2022-04, Vol.262-263, p.111-117

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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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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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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Spectrum of cytomorphological features, including literature review, of an extraskeletal myxoid chondrosarcoma with t(9;22)(q22;q12) (TEC/EWS) results in one case

Diagnostic cytopathology, 2008-12, Vol.36 (12), p.868-875

2008

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RUNX1 ABERRATIONS IN ETV6/RUNX1-POSITIVE AND ETV6/RUNX1-NEGATIVE PATIENTS: Its Hemato-Pathological and Prognostic Significance in a Large Cohort (619 Cases) of ALL

Pediatric hematology and oncology, 2008-01, Vol.25 (6), p.582-597

2008

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Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia

Leukemia research, 2005-05, Vol.29 (5), p.517-526

2005

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Coexistence of ETV6/RUNX1 and MLL aberrations in B-cell precursor acute lymphoblastic leukemia discloses a small subclass of BCP-ALL

Cancer genetics and cytogenetics, 2008-04, Vol.182 (1), p.27-32

2008

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A Case of Partial Trisomy of 10q and Partial Monosomy of 6p Resulting from Maternal t(6;10) (p23;q24)

Atypical Co-amplification with Co-localization of HER2 Gene in Breast Cancer: Combined IHC/FISH Approach as per ASCO/CAP 2018 Guidelines for Targeted Therapy Eligibility

Atypical MYC rearrangement pattern of 3′ deletion and 5′ amplification along with independent IGH rearrangement: A case study

Derivative 6 as an additional chromosomal abnormality along with t(15;17): A case report

Tetrasomy 8 in Haematological Malignancies-A Case Series

Pentasomy X Syndrome in Neonate: A Rare Disorder

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

Derivative 6 as an additional chromosomal abnormality along with t

A novel coexistence of tetrasomy 8 and FLT3-ITD along with variant 3 way translocation t(4;17;15) in acute promyelocytic leukemia: Case study and literature review

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

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

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

Spectrum of cytomorphological features, including literature review, of an extraskeletal myxoid chondrosarcoma with t(9;22)(q22;q12) (TEC/EWS) results in one case

RUNX1 ABERRATIONS IN ETV6/RUNX1-POSITIVE AND ETV6/RUNX1-NEGATIVE PATIENTS: Its Hemato-Pathological and Prognostic Significance in a Large Cohort (619 Cases) of ALL

Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia

Coexistence of ETV6/RUNX1 and MLL aberrations in B-cell precursor acute lymphoblastic leukemia discloses a small subclass of BCP-ALL

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