Analysis of 17 Prenatal Cases with the Chromosomal 1q21.1 Copy Number Variation

Copy number variations (CNVs) at the chromosomal 1q21.1 region represent a group of hot-spot recurrent rearrangements in human genome, which have been detected in hundreds of patients with variable clinical manifestations. Yet, report of such CNVs in prenatal scenario was relatively scattered. In th...

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Detalles Bibliográficos
Autores principales: Wen, Xiaohui, Xing, Huanxia, Qi, Keyan, Wang, Hao, Li, Xiaojun, Zhu, Jianjiang, Chen, Wenqi, Cui, Limin, Zhang, Jing, Qi, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241571/
https://www.ncbi.nlm.nih.gov/pubmed/37284664
http://dx.doi.org/10.1155/2022/5487452

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241571/
https://www.ncbi.nlm.nih.gov/pubmed/37284664
http://dx.doi.org/10.1155/2022/5487452

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