Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders

Chromosome 15q24 microdeletion is a rare genetic disorder characterized by development delay, facial dysmorphism, congenital malformations, and occasional autism spectrum disorder (ASD). In this study, we identified five cases of 15q24 microdeletion using multiplex ligation-dependent probe amplifica...

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Detalles Bibliográficos
Autores principales: Zhang, Yuanyuan, Liu, Xiaoliang, Gao, Haiming, Cui, Wanting, Zhang, Bijun, Zhao, Yanyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684056/
https://www.ncbi.nlm.nih.gov/pubmed/34922566
http://dx.doi.org/10.1186/s13039-021-00574-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684056/
https://www.ncbi.nlm.nih.gov/pubmed/34922566
http://dx.doi.org/10.1186/s13039-021-00574-x

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