TY - JOUR AU - Szelest, Monika AU - Stefaniak, Martyna AU - Ręka, Gabriela AU - Jaszczuk, Ilona AU - Lejman, Monika PY - 2021 DA - 2021/03/10 TI - Three case reports of patients indicating the diversity of molecular and clinical features of 16p11.2 microdeletion anomaly JO - BMC Medical Genomics SP - 76 VL - 14 IS - 1 AB - 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 among the general population, it is one of the serious known genetic aetiologies of obesity and autism spectrum disorder. SN - 1755-8794 UR - https://doi.org/10.1186/s12920-021-00929-8 DO - 10.1186/s12920-021-00929-8 ID - Szelest2021 ER -