Associated Papers
CTCF/RAD21 organize the ground state of chromatin-nuclear speckle association.
Yu R et al.
Nature Structural & Molecular Biology, 2025
Clinical Characteristics, Genetic Analysis, and Literature Review of Cornelia de Lange Syndrome Type 4 Associated With a RAD21 Variant.
Yue X et al.
Molecular Genetics & Genomic Medicine, 2024
Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis.
Abarca-Barriga HH et al.
Genes, 2023
CTCF/cohesin organize the ground state of chromatin-nuclear speckle association.
Yu R et al.
Biorxiv : the Preprint Server for Biology, 2023
Delineation of phenotypes and genotypes related to cohesin structural protein RAD21.
Krab LC et al.
Human Genetics, 2020
A genome-wide DNA methylation signature for SETD1B-related syndrome.
Krzyzewska IM et al.
Clinical Epigenetics, 2019
31685013 (PubMed )
Supplement: 13148_2019_749_MOESM5_ESM.xlsx › Sheet1
Cohesin complex-associated holoprosencephaly.
Kruszka P et al.
Brain : a Journal of Neurology, 2019
A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4 - Review of the literature.
Gudmundsson S et al.
European Journal of Medical Genetics, 2019
A novel RAD21 variant associated with intrafamilial phenotypic variation in Cornelia de Lange syndrome - review of the literature.
Boyle MI et al.
Clinical Genetics, 2017
Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case.
Minor A et al.
Gene, 2014
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