De novo 22q11.2 deletions and auricular findings in two Chinese patients with microtia

BACKGROUND: Congenital microtia is a common craniofacial malformation resulting from both environmental and genetic factors. Recurrent chromosomal imbalances were observed in patients with microtia. The 22q11.2 deletion is one of the most common microdeletions in human beings. The cell division cycl...

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Detalles Bibliográficos
Autores principales: Si, Nuo, Zhang, Zeya, Huang, Xin, Wang, Chanchen, Guo, Peipei, Pan, Bo, Jiang, Haiyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801138/
https://www.ncbi.nlm.nih.gov/pubmed/34971493
http://dx.doi.org/10.1002/mgg3.1862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801138/
https://www.ncbi.nlm.nih.gov/pubmed/34971493
http://dx.doi.org/10.1002/mgg3.1862

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