1. Akbas H, Cine N, Erdemoglu M, Atay AE, Simsek S, Turkyilmaz A, et al. Prenatal diagnosis of 4p and 4q subtelomeric microdeletion in de novo ring chromosome 4. Case Rep Obstet Gynecol. 2013;2013:248050.
2. Balikova I, Menten B, de Ravel T, Le Caignec C, Thienpont B, Urbina M, et al. Subtelomeric imbalances in phenotypically normal individuals. Hum Mutat. 2007;28(10):958–67.
3. Barrie ES, Cottrell CE, Gastier-Foster J, Hickey SE, Patel AD, Santoro SL, et al. Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 gene. Eur J Med Genet. 2020;63(3):103735.
4. Descartes M, Keppler-Noreuil K, Knops J, Longshore JW, Finley WH, Carroll AJ. Terminal deletion of the long arm of chromosome 4 in a mother and two sons. Clin Genet. 1996;50(6):538–40.
5. Fu F, Chen F, Li R, Zhang Y, Pan M, Li D, et al. Prenatal diagnosis of fetal multicystic dysplastic kidney via high-resolution whole-genome array. Nephrol Dial Transplant. 2016;31(10):1693–8.