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

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 phenotypi...

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Detalles Bibliográficos
Autores principales: Yang, Huanhuan, Huang, Jun, Zheng, Hao, Zhang, Yunfan, Zhang, Yuanzhen, Liu, Wei, Wu, Jinrong, Chen, Xiaobin, Lin, Jinfeng, Ni, Yanna, Nie, Xiaojing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634020/
https://www.ncbi.nlm.nih.gov/pubmed/37946214
http://dx.doi.org/10.1186/s12920-023-01723-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634020/
https://www.ncbi.nlm.nih.gov/pubmed/37946214
http://dx.doi.org/10.1186/s12920-023-01723-4

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