{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n The abstract (1) details a case of a 14‐year‐old girl with multiple congenital anomalies and developmental delay, attributed to complex chromosomal rearrangements involving chromosomes 3, 7, and 12. The genomic investigations revealed several structural aberrations, including an inversion, insertions, translocations, and two submicroscopic deletions. One of these deletions disrupts the ROBO1 gene—a candidate contributing to neurodevelopmental deficits—while additional factors such as gene disruption and position effects may further influence the phenotype. Notably, the abstract does not mention or provide any information regarding the function of BCDIN3D‑AS1.\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Citation:."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Morteza Hemmat, Xiaojing Yang, Patricia Chan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Characterization of a complex chromosomal rearrangement using chromosome, FISH, and microarray assays in a girl with multiple congenital abnormalities and developmental delay."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cytogenet (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/1755-8166-7-50"}], "href": "https://doi.org/10.1186/1755-8166-7-50"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25478007"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25478007"}]}]}]}