Correspondence on “De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females” by Polla et al.
- 1 October 2021
- journal article
- letter
- Published by Elsevier BV in Genetics in Medicine
- Vol. 23 (10), 2003-2004
- https://doi.org/10.1038/s41436-021-01208-8
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 femalesGenetics in Medicine, 2020
- De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in femalesGenetics in Medicine, 2020
- The power of the Mediator complex—Expanding the genetic architecture and phenotypic spectrum of MED12‐related disordersClinical Genetics, 2018
- Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation PatternHuman Mutation, 2016