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pro vyhledávání: '"Pallavi Suresh Laddha"'
Autor:
Sandhya Devi G., Faiq Ahmed, Manasi C. Mundada, Rachna Khera, Lavanya Nambaru, Krishnamohan Mallavarapu, Pavan Kumar Boyella, Veerandra Patil, Pallavi Suresh Laddha, Senthil J. Rajappa
Publikováno v:
Indian Journal of Medical and Paediatric Oncology.
Introduction Translocation t(12;21)(p13;q22), a recurrent and an invisible chromosomal abnormality, resulting in TEL/AML1 gene fusion, associated with good prognosis, has been described to be a common abnormality, in children with B-acute lymphoblast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::461acf3469ebf50a9a2d98e5e8d66a89
https://doi.org/10.1055/s-0042-1742611
https://doi.org/10.1055/s-0042-1742611
