Familial Translocation t(2;4) (q37.3;p16.3), Resulting in a Partial Trisomy of 2q (or 4p) and a Partial Monosomy of 4p (or 2q), Causes Dysplasia

Background: Wolf-Hirschhorn syndrome, a well-known contiguous microdeletion syndrome, is caused by deletions on chromosome 4p. While the clinical symptoms and the critical region for this disorder have been identified based on genotype-phenotype correlations, duplications in this region have been in...

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Detalles Bibliográficos
Autores principales: Wang, Jian, Zhou, Shiyuan, He, Fei, Zhang, Xuelian, Lu, Jianqi, Zhang, Jian, Zhang, Feng, Xu, Xiangmin, Yang, Fang, Xiong, Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650131/
https://www.ncbi.nlm.nih.gov/pubmed/34887900
http://dx.doi.org/10.3389/fgene.2021.741607

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650131/
https://www.ncbi.nlm.nih.gov/pubmed/34887900
http://dx.doi.org/10.3389/fgene.2021.741607

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