A novel chromosome 2q24.3‐q32.1 microdeletion in a fetus with multiple malformations

BACKGROUND: Terminal or interstitial deletion of chromosome 2q is rarely reported but clinically significant, which can result in developmental malformations and psychomotor retardation in humans. In the present study, we analyzed this deletion to comprehensively clarify the relationship between phe...

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Detalles Bibliográficos
Autores principales: Zhu, Mianmian, Wang, Yihong, Guan, Lijie, Lu, Chaosheng, Sun, Rongyue, Chen, Yuan, Shi, Jiamin, Zhu, Yanying, Wang, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396185/
https://www.ncbi.nlm.nih.gov/pubmed/35819063
http://dx.doi.org/10.1002/jcla.24602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396185/
https://www.ncbi.nlm.nih.gov/pubmed/35819063
http://dx.doi.org/10.1002/jcla.24602

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