Chromosome 22q11.21 and 11p15.4 microdeletions confirmed by high‐throughput sequencing analysis in one patient with asymmetric cry syndrome: Case report and review of the literature

Healthcare providers treating newborns with asymmetric cry syndrome should consider 22q11.2 microdeletion within the differential diagnosis list and order appropriate genetic testing.

Detalles Bibliográficos
Autores principales: Pang, Yonghong, Yu, Yang, Deng, Xiaoyi, Liu, Qian, Yan, Junmei, Gao, Xiangyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142403/
https://www.ncbi.nlm.nih.gov/pubmed/34084494
http://dx.doi.org/10.1002/ccr3.4072

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8142403/
https://www.ncbi.nlm.nih.gov/pubmed/34084494
http://dx.doi.org/10.1002/ccr3.4072

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