A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability

• Main Authors: Živilė Maldžienė (Author), Evelina M. Vaitėnienė (Author), Beata Aleksiūnienė (Author), Algirdas Utkus (Author), Eglė Preikšaitienė (Author)
• Format: Book
• Published: BMC, 2020-04-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Interstitial 4q deletions are rare chromosomal alterations. Most of the previously reported deletions involving the 4q13.3 region are large chromosomal alterations with a common loss of band 4q21 resulting in marked growth restriction, severe intellectual disability, and absent o...