Cargando…
Enigmatic Inv(9): A Case Report on Rare Findings in Hematological Malignancies
INTRODUCTION: Inversion of chromosome 9 had been widely discussed among geneticists and evolutionary biologists because of its significant impact on various hereditary disorders and in the evolution of man. The role of such inversions in human disease evolution is an area hitherto unclear. CASE PRES...
Autores principales: | Vijay, Sangeetha, Narayanan, Geetha, Sarojam, Santhi, Raveendran, Suresh Kumar, Hariharan, Sreedharan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895997/ https://www.ncbi.nlm.nih.gov/pubmed/27280043 http://dx.doi.org/10.5812/ircmj.25062 |
Ejemplares similares
-
A novel chromosomal abnormality t (9;14)(p24;q13) in B-acute lymphoblastic leukemia
por: Raveendran, Sureshkumar, et al.
Publicado: (2014) -
Recurrent isochromosome 21 and multiple abnormalities in a patient suspected of having acute myeloid leukemia with eosinophilic differentiation—a rare case from South India
por: Vijay, Sangeetha, et al.
Publicado: (2012) -
Novel t(7;10)(p22;p24) along with NPM1 mutation in patient with relapsed acute myeloid leukemia
por: Sarojam, Santhi, et al.
Publicado: (2013) -
Characteristics of hematologic malignancies with coexisting t(9;22) and inv(16) chromosomal abnormalities
por: Han, Eunhee, et al.
Publicado: (2014) -
Prognostic Implications of DNA Repair, Ploidy and Telomerase in the Malignant Transformation Risk Assessment of Leukoplakia
por: Thomas, Gigi, et al.
Publicado: (2020)