Search Results - "DEV, VAITHILINGAM G"

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    Interphase Chromosome Profiling: A Method for Conventional Banded Chromosome Analysis Using Interphase Nuclei by Babu, Ramesh, Van Dyke, Daniel L, Dev, Vaithilingam G, Koduru, Prasad, Rao, Nagesh, Mitter, Navnit S, Liu, Mingya, Fuentes, Ernesto, Fuentes, Sarah, Papa, Stephen

    “…- Chromosome analysis on bone marrow or peripheral blood samples fails in a small proportion of attempts. A method that is more reliable, with similar or…”
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    Frequency of FLT3 – internal tandem duplication (ITD) gene mutations in various cytogenetic groups in acute myelogenous leukemia (AML): A report from Tamil Nadu, India by Elangovan, Kanimozhi, Li, Nenggan, Gu, Guangyu, Dev, Vaithilingam G., Thangaraju, Palanimuthu

    Published in Gene reports (01-12-2021)
    “…To standardize simple PCR based technique to identify FLT3 mutations in patients with newly diagnosed acute myelogenous leukemia (AML). Thirty six patients…”
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    A novel t(2;20)(q35;p12) in embryonal rhabdomyosarcoma by Ho, Richard H, Johnson, Joyce, Dev, Vaithilingam G, Whitlock, James A

    Published in Cancer genetics and cytogenetics (01-05-2004)
    “…Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood, accounting for 5%–8% of all pediatric malignancies. RMS can be categorized into…”
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    Expression of Human and Suppression of Mouse Nucleolus Organizer Activity in Mouse-Human Somatic Cell Hybrids by Miller, Orlando J., Miller, Dorothy A., Dev, Vaithilingam G., Tantravahi, Ramana, Croce, Carlo M.

    “…Most mouse-human somatic cell hybrids show preferential loss of human chromosomes, absence of human 28S ribosomal RNA, and suppression of human nucleolus…”
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    Reactivation of Silent rRNA Genes by Simian Virus 40 in Human-Mouse Hybrid Cells by Soprano, Kenneth J., Dev, Vaithilingam G., Croce, Carlo M., Baserga, Renato

    “…Mouse-human hybrid cells were used to study the ability of simian virus 40 to regulate the expression of rRNA genes in vivo. In these hybrid cells, only the…”
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    Direct karyotyping of unstimulated newborn blood: A rapid diagnostic method for the clinical management of critically ill newborns by Tharapel, Sugandhi A., Dev, Vaithilingam G.

    Published in American journal of medical genetics (31-10-1997)
    “…Using spontaneously dividing nucleated erythrocytes present in newborn cord and peripheral blood, we performed direct karyotype analysis on a cohort of 162…”
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    Counseling and decision dilemmas associated with fetal blood sampling by Ulm, J E, Shah, D M, Dev, V G, Phillips, 3rd, J A

    Published in American journal of medical genetics (01-01-1990)
    “…Counseling before fetal blood sampling via cordocentesis is more difficult than that done before amniocentesis because 1) a fetal anomaly has been detected or…”
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    Unusual translocations t(2;6) and t(?;22) in a child with acute myelocytic leukemia by Dev, V G, Carroll, A J, Crist, W M, Peterson, R D, Mankad, V N

    Published in Cancer genetics and cytogenetics (01-01-1983)
    “…A 13-month-old female with middle and upper lobe pneumonia showed a high WBC count with 99% blasts. From hematologic studies the condition was diagnosed as…”
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  16. 16

    The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis by Butler, M G, Dev, V G, Shah, D, Ulm, J E, Wilmot, P L, Shapiro, L R

    Published in American journal of medical genetics (01-12-1988)
    “…Early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal diagnosis were undertaken for the first time in a 17-week…”
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