Adverse Perinatal and Early Life Outcomes following 15q11.2 CNV Diagnosis

The copy number variation (CNV) of 15q11.2, an emerging and common condition observed during prenatal counseling, is encompassed by four highly conserved and non-imprinted genes—TUBGCP5, CYFIP1, NIPA1, and NIPA2—which are reportedly related to developmental delays or general behavioral problems. We...

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Detalles Bibliográficos
Autores principales: Chu, Fu-Chieh, Shaw, Steven W., Lee, Chien-Hong, Lo, Liang-Ming, Hsu, Jenn-Jeih, Hung, Tai-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535766/
https://www.ncbi.nlm.nih.gov/pubmed/34680874
http://dx.doi.org/10.3390/genes12101480

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535766/
https://www.ncbi.nlm.nih.gov/pubmed/34680874
http://dx.doi.org/10.3390/genes12101480

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