Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1

The subchromosomal region 1q21.1 is one of the hotspots in the human genome for deletions and reciprocal duplications, owing to the existence of hundreds of segmental duplications. Recurrent deletions and duplications in this region are thought to be causative in patients with variable clinical mani...

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Detalles Bibliográficos
Autores principales: Pang, Hui, Yu, Xiaowei, Kim, Young Mi, Wang, Xianfu, Jinkins, Jeremy K., Yin, Jianing, Li, Shibo, Gu, Hongcang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325322/
https://www.ncbi.nlm.nih.gov/pubmed/32655619
http://dx.doi.org/10.3389/fgene.2020.00577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325322/
https://www.ncbi.nlm.nih.gov/pubmed/32655619
http://dx.doi.org/10.3389/fgene.2020.00577

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