Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees

Background: Chromosomal aberrations contribute to human phenotypic diversity and disease susceptibility, but it is difficult to assess their pathogenic effects in the clinic. Therefore, it is of great value to report new cases of chromosomal aberrations associated with normal phenotypes or clinical...

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Detalles Bibliográficos
Autores principales: Hu, Huamei, Zhang, Rong, Ma, Yongyi, Luo, Yanmei, Pan, Yan, Xu, Juchun, Jiang, Lupin, Wang, Dan
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/PMC8724545/
https://www.ncbi.nlm.nih.gov/pubmed/34992628
http://dx.doi.org/10.3389/fgene.2021.731815

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724545/
https://www.ncbi.nlm.nih.gov/pubmed/34992628
http://dx.doi.org/10.3389/fgene.2021.731815

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