Phenotypic features of a microdeletion in chromosome band 20p13: A case report and review of the literature

BACKGROUND: 20p13 microdeletion syndrome has been reported to be associated with developmental delays, intellectual disability, epilepsy, and unspecific dysmorphic characteristics. However, only a few cases of 20p13 microdeletion have been described, and therefore its typical features and precise pa...

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Detalles Bibliográficos
Autores principales: Fang, Hung‐Hsiang, Liu, Shih‐Yao, Wang, Ying‐Fu, Chiang, Che‐Ming, Liu, Chiung‐Chen, Lin, Chien‐Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625104/
https://www.ncbi.nlm.nih.gov/pubmed/31087544
http://dx.doi.org/10.1002/mgg3.739

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625104/
https://www.ncbi.nlm.nih.gov/pubmed/31087544
http://dx.doi.org/10.1002/mgg3.739

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