Search Results - "Kerketta, Lily"

Centrosome Aberration Frequency and Disease Association in B-Acute Lymphoblastic Leukemia by Kerketta, Lily S, Ghosh, Kanjaksha, Nadkarni, Anita, Madkaikar, Manisha, Vundinti, Babu Rao

“…Recent developments in genome-wide genetic analysis in B-acute lymphoblastic leukemia (B-ALL) have provided insight into disease pathogenesis and prognosis…”
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Chromosomal aberrations in primary amenorrhea: A retrospective study by Korgaonkar, Seema, Dhangar, Somprakash, Kulkarni, Vinayak, Kerketta, Lily, Vundinti, Babu

“…Objectives: The aim of this study was to estimate the frequency of chromosomal abnormalities and establish the association with clinical of factors such as…”
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Standard karyotyping concentrates microfilaria and can be a valid concentrating technique for their detection by Kerketta, Lily S., Rao, Vundinti Babu, Ghosh, Kanjaksha

“…During karyotype preparation from the bone marrow aspirates of 209 haematological malignancy cases, microfilaria were detected in four samples, whereas routine…”
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Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymhoblastic leukemia cases from India by Kerketta, Lily S, Baburao, Vundinti, Ghosh, Kanjaksha

“…Hyperdiploid pre-B-cell acute lymhoblastic leukemia (pre-B-ALL) is a common form of childhood leukemia with very good prognosis with present day chemotherapy…”
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Chimeric fusion karyotypes in childhood B-cell acute lymphoblastic leukemia by Kerketta, Lily S, Rao, Vundinti Babu, Ghosh, Kanjaksha

“…Cytogenetics study using combination of conventional cytogenetics and fluorescent insitu hybridization was carried out in 171 pediatric acute lymphoblastic…”
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FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India by Ghosh, Kanjaksha, Swaminathan, Suchitra, Madkaikar, Manisha, Gupta, Maya, Kerketta, Lily, Vundinti, Baburao

“…Acute myeloid leukemia (AML) is an aggressive hematological disorder characterized by the loss of ability of the hematopoietic progenitor cells to…”
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Standard karyotyping concentrates microfilaria and can be a valid concentrating technique for their detection; Le caryotypage standard concentre les microfilaires et peut être une technique viable de concentration pour leur détection; El cariotipado estándar concentra las microfilarias y podría ser una técnica de concentración viable para su detección by Kerketta, Lily S, Rao, Vundinti Babu, Ghosh, Kanjaksha

“…During karyotype preparation from the bone marrow aspirates of 209 hematological malignancy cases, microfilaria were detected in four samples, whereas routine…”
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Prevalence and Association of Dermatological Manifestations with Fanconi Anemia: A Retrospective Study by Shukla, Pallavi, Korgaonkar, Seema, Kerketta, Lily, Vundinti, Babu R

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Research Letters by Juneja, Monica, Sairam, Smitha, Jain, Rahul, Kerketta, Lily S., Rao, Vundinti Babu, Ghosh, Kanjaksha

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Cytogenetic study of myelodysplastic syndrome from India by Vundinti, Babu Rao, Kerketta, Lily, Jijina, Farah, Ghosh, K

“…Myelodysplastic syndrome (MDS) represents a group of clonal haematological disorders characterized by progressive cytopenia reflecting defects in erythroid,…”
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Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation by Swaminathan, Suchitra, Madkaikar, Manisha, Ghosh, Kanjaksha, Vundinti, Babu Rao, Kerketta, Lily, Gupta, Maya

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Translocation t(2;14)(p13;q32) in a case of Ph+ acute lymphoblastic leukemia by Kerketta, Lily, Vundinti, Babu Rao, Ghosh, Kanjaksha

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DNA copy number changes and immunophenotype pattern in karyotypically normal acute myeloid leukemia patients from an Indian population by Kawankar, Nikesh, Korgaonkar, Seema, Kerketta, Lily, Madkaikar, Manisha, Jijina, Farah, Ghosh, Kanjaksha, Vundinti, Babu Rao

“…Chromosomal abnormalities are important in the diagnosis and prognosis of patients with acute myeloid leukemia (AML). The purpose of this study was to identify…”
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Chromosomal breakage in myelodysplatic syndrome by Korgaonkar, Seema, Babu, V Rao, Kerketta, Lily, Ghosh, Kanjaksha

“…The myelodysplastic syndrome (MDS) represents a group of clonal hematological disorders characterized by progressive cytopenia reflecting defects in erythroid,…”
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Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases by Rao, Babu, Kerketta, Lily, Korgaonkar, Seema, Ghosh, Kanjaksha

“…Background: The chromosomal polymorphism of short arms of acrocentric chromosomes and heterochromatin variation of Chromosomes 1, 9, 16 and Y have been…”
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Case Report - Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3) by Vundinti, Babu Rao, Kerketta, Lily, Korgaonkar, Seema, Ghosh, Kanjaksha

“…We describe a five-year-old proband presented with Dandy-Walker malformations, right microopthalmia, hamstring contractures, undescended testis with absence of…”
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Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases by Rao BabuV, Kerketta Lily, Korgaonkar Seema, Ghosh Kanjaksha

“…Background: The chromosomal polymorphism of short arms of acrocentric chromosomes and heterochromatin variation of Chromosomes 1, 9, 16 and Y have been…”
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Dandy-Walker malformations in a case of partial trisomy 9p by Vundinti, Babu Rao, Kerketta, Lily, Korgaonkar, Seema, Ghosh, Kanjaksha

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Translocation t(2;14)(p13;q32) in a case of Ph+ acute lymphoblastic leukemia by Kerketta, Lily, Vundinti, Babu Rao, Ghosh, Kanjaksha

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Hybrid cytogenetics of chronic lymphocytic leukemia and follicular cell lymphoma in a case of non-Hodgkin's lymphoma by Babu Rao, V, Kerketta, Lily, Madkaikar, M, Farah, J, Ghosh, K

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