Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies

Background: The phenotype of duplication of 1q21.1 region is variable, ranging from macrocephaly, autism spectrum disorder, congenital anomalies, to a normal phenotype. Few cases have been reported in the literature regarding prenatal diagnosis of 1q21.1 duplication syndrome. The current study prese...

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Detalles Bibliográficos
Autores principales: Ji, Xiuqing, Pan, Qiong, Wang, Yan, Wu, Yun, Zhou, Jing, Liu, An, Qiao, Fengchang, Ma, Dingyuan, Hu, Ping, Xu, Zhengfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109635/
https://www.ncbi.nlm.nih.gov/pubmed/30177949
http://dx.doi.org/10.3389/fgene.2018.00275

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109635/
https://www.ncbi.nlm.nih.gov/pubmed/30177949
http://dx.doi.org/10.3389/fgene.2018.00275

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