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

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 or severe...

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Detalles Bibliográficos
Autores principales: Maldžienė, Živilė, Vaitėnienė, Evelina M., Aleksiūnienė, Beata, Utkus, Algirdas, Preikšaitienė, Eglė
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160938/
https://www.ncbi.nlm.nih.gov/pubmed/32299451
http://dx.doi.org/10.1186/s12920-020-0711-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160938/
https://www.ncbi.nlm.nih.gov/pubmed/32299451
http://dx.doi.org/10.1186/s12920-020-0711-4

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