Cytogenetics' impact on the prognosis of acute myeloid leukemia by Monika Gupta, Manoranjan Mahapatra, Renu Saxena

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A rare case of double heterozygous state for HbD and HbE by Sanjeev Kumar Gupta, Jasmita Dass, Renu Saxena

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G6PD deficiency in females screened at tertiary care hospital by Monica Sharma, Jasmita Dass, Bhavna Dhingra, Renu Saxena

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Transfusion-acquired Hemoglobinopathies: A Report of Two Cases by Venkatesan Somasundaram, Abhishek Purohit, Prabhu Manivannan, Renu Saxena

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Trisomy Chromosome 6 as a Sole Cytogenetic Abnormality in Acute Myeloid Leukemia by Monika  Gupta, Nita  Radhakrishnan, Manoranjan Mahapatra, Renu Saxena

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MODULATING EFFECT OF THE −158 GΓ (C→T) XMN-1 POLYMORPHISM IN INDIAN SICKLE CELL PATIENTS by Sanjay Pandey, Sweta Pandey, Rahasya Mani Mishra, Renu Saxena

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Scleredema-associated IgA myeloma with myelofibrosis in a young adult: a case report by Renu Saxena, Hara Prasad Pati, Rakhee Kar, Seema Rao

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Evaluation of bone mineral density (BMD) and the effect of type of factor replacement therapy on BMD in children with hemophilia: A single-center observational study by Govind R. Patel, Renu Saxena, Sadhna Aggarwal, Manoranjan Mahapatra

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Serial values of hematologic variables and deep venous thrombosis: Red cell distribution width is associated with deep venous thrombosis by Govind R. Patel, Manoranjan Mahapatra, Sadhna Aggarwal, Renu Saxena

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Atypical immunophenotype of T-cell Acute Lymphoblastic Leukemia by Abhishek Purohit, Mukul Aggarwal, Hara P Pati, Renu Saxena

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Current state of non-hematologic cancer-associated thrombosis at a tertiary care hospital in India by Mukul Aggarwal, Amrita Ramaswami, Manoranjan Mahapatra, Seema Tyagi, Renu Saxena

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Crigler Najjar Syndrome Type 2 (CNS Type 2): An Unwonted Cause of Jaundice in Adults by Prabhat Kumar, Gargi Sasmal, Shreya Gupta, Renu Saxena, Sudha Kohli

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Implications of CYP21A2 gene duplications in carrier screening and prenatal diagnosis of congenital adrenal hyperplasia due to 21 Hydroxylase deficiency by Sudhisha Dubey, Renu Saxena, Ratna Dua Puri, Ishwar Chander Verma

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Association of JAK2V617F mutation with thrombosis in Indian patients with Philadelphia negative chronic myeloproliferative neoplasms by Kanwaljeet Singh, Sudha Sazawal, Sunita Chhikara, Manoranjan Mahapatra, Renu Saxena

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Study of Bone Marrow Lymphocyte Subset in Acute Myeloid Leukemia by Prasad Dange, Seema Tyagi, Richa Juneja, Tulika Seth, Renu Saxena

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Establishing a normal reference range for thromboelastography in North Indian healthy volunteers by Arulselvi Subramanian, Venencia Albert, Renu Saxena, Deepak Agrawal, Ravindra Mohan Pandey

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Homozygous ?- thalassemia with Glucose 6 phosphate dehydrogenase deficiency: A case report. by Jitender Mohan Khunger, Rohit Kapoor, Rekha Singh, Monica Khunger, Renu Saxena

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Griscelli syndrome type 2: a novel mutation in gene with different clinical features in 2 siblings: a diagnostic conundrum by Kirtisudha Mishra, Shilpy Singla, Suvasini Sharma, Renu Saxena, Vineeta Vijay Batra

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LMNB1 duplication-mediated autosomal dominant adult-onset leukodystrophy in an Indian family by Sunita Bijarnia-Mahay, Gaurav Roy, Quasar S Padiath, Renu Saxena, Ishwar Chander Verma

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Effect of directly observed oral iron supplementation during pregnancy on iron status in a rural population in Haryana: A randomized controlled trial by Farhad Ahamed, Kapil Yadav, Shashi Kant, Renu Saxena, Mohan Bairwa, Chandrakant S Pandav

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