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  1. Article

    Open Access

    Hypodiploidy in a pediatric patient of T-cell acute lymphoblastic leukemia: a case report

    T-cell acute lymphoblastic leukemia is a subtype of acute lymphoblastic leukemia, one of the most common childhood neoplasms. Hypodiploidy is a chromosome abnormality with fewer than 45 chromosomes and is asso...

    Martyna Stefaniak, Gabriela Ręka, Joanna Zawitkowska, Monika Lejman in BMC Medical Genomics (2021)

  2. Article

    Open Access

    Three case reports of patients indicating the diversity of molecular and clinical features of 16p11.2 microdeletion anomaly

    16p11.2 microdeletion is a known chromosomal anomaly associated mainly with neurocognitive developmental delay, predisposition to obesity, and variable dysmorphism. Although this deletion is relatively rare am...

    Monika Szelest, Martyna Stefaniak, Gabriela Ręka, Ilona Jaszczuk in BMC Medical Genomics (2021)