Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report

1P36 deletion syndrome is recognized as the most common terminal microdeletion syndrome in humans, characterized by early developmental delay and consequent intellectual disability, seizure disorder, and disti...

Source: BMC Medical Genomics - November 9, 2023 Category: Genetics & Stem Cells Authors: Huanhuan Yang, Jun Huang, Hao Zheng, Yunfan Zhang, Yuanzhen Zhang, Wei Liu, Jinrong Wu, Xiaobin Chen, Jinfeng Lin, Yanna Ni and Xiaojing Nie Tags: Case Report Source Type: research