This section considers studies of change in the expression and regulation of genes and genomes by genetic and epigenetic mechanisms in relation to human health and disease states.
A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability
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 ...
Citation: BMC Medical Genomics 2020 13:63