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

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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Bibliographic Details
Main Authors: Idit Maya, Sharon Perlman, Mordechai Shohat, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifaat Agmon-Fishman, Reut Tomashov Matar, Lina Basel-Salmon, Rivka Sukenik-Halevy
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Journal of Clinical Medicine
Subjects:
chromosomal microarray
phenotype
BP1-BP2
15q11.2
deletions
duplications
Online Access:https://www.mdpi.com/2077-0383/9/8/2602

Internet

https://www.mdpi.com/2077-0383/9/8/2602

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