Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference14 articles.
1. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
2. Controlling elements in the mouseX-chromosome: I. Interaction with the X-linked genes
3. Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups
4. Clonal analysis of human tumors with M27 beta, a highly informative polymorphic X chromosomal probe.
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1. Comprehensive genomic filtering algorithm to expose the cause of skewed X chromosome inactivation. The proof of concept in female haemophilia expression;Journal of Medical Genetics;2024-05-06
2. A quantum mechanical approach to random X chromosome inactivation;AIMS Biophysics;2021
3. Α de novo 3.8-Mb inversion affecting the EDA and XIST genes in a heterozygous female calf with generalized hypohidrotic ectodermal dysplasia;BMC Genomics;2019-09-18
4. Phenotype-genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X-chromosome inactivation;Journal of Thrombosis and Haemostasis;2015-03-14
5. Analysis of C43G mutation in the promoter region of theXISTgene in patients with idiopathic primary ovarian insufficiency;Clinical and Experimental Reproductive Medicine;2015
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