Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?

Copy number variations of the 15q11.2 region at breakpoints 1-2 (BP1-BP2) have been associated with variable phenotypes and low penetrance. Detection of such variations in the prenatal setting can result in significant parental anxiety. The clinical significance of pre- and postnatally detected 15q1...

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Detalles Bibliográficos
Autores principales: Maya, Idit, Perlman, Sharon, Shohat, Mordechai, Kahana, Sarit, Yacobson, Shiri, Tenne, Tamar, Agmon-Fishman, Ifaat, Tomashov Matar, Reut, Basel-Salmon, Lina, Sukenik-Halevy, Rivka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463673/
https://www.ncbi.nlm.nih.gov/pubmed/32796639
http://dx.doi.org/10.3390/jcm9082602

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463673/
https://www.ncbi.nlm.nih.gov/pubmed/32796639
http://dx.doi.org/10.3390/jcm9082602

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