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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| 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 |