Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2

Copy number variations (CNVs) in chromosome 16p11.2 (deletions and duplications) are not rare. 16p11.2 microdeletion is among the most commonly known genetic etiologies of autism spectrum disorder, overweightness, and related neurodevelopmental disorders. Here, we report the prenatal diagnosis and g...

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Detalles Bibliográficos
Autores principales: Li, Meihua, Liu, Linlin, Wu, Yijun, Guan, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Retrospective Clinical Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274417/
https://www.ncbi.nlm.nih.gov/pubmed/35808818
http://dx.doi.org/10.1177/03000605221109400

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9274417/
https://www.ncbi.nlm.nih.gov/pubmed/35808818
http://dx.doi.org/10.1177/03000605221109400

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