Related Articles
Proximal 10q duplication in a child with severe central hypotonia characterized by array‑comparative genomic hybridization: A case report and review of the literature
Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report
MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report
Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report
A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): A case report