Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

Overview of attention for article published in Molecular Cytogenetics, November 2013

Altmetric Badge

About this Attention Score

Average Attention Score compared to outputs of the same age
Good Attention Score compared to outputs of the same age and source (73rd percentile)

So far, Dimensions has found 25 publications that cite this research output.

Article in Genes (February 2024)

Article in Molecular Cytogenetics (January 2023)

Article in Molecular Cytogenetics (August 2022)

This page shows the most recent citations of this research output.

Click here to find out how to access more activity.