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

• Main Authors: Huanhuan Yang (Author), Jun Huang (Author), Hao Zheng (Author), Yunfan Zhang (Author), Yuanzhen Zhang (Author), Wei Liu (Author), Jinrong Wu (Author), Xiaobin Chen (Author), Jinfeng Lin (Author), Yanna Ni (Author), Xiaojing Nie (Author)
• Format: Book
• Published: BMC, 2023-11-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background 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 distinctive facial features. Variable deletion locations may attributed to p...