![Allelic association results and linkage disequilibrium (LD) plot of the chromosome Xq28 region around the MECP2 gene. Allelic association results and linkage disequilibrium (LD) plot of the chromosome Xq28 region around the MECP2 gene.](https://s3-eu-west-1.amazonaws.com/ppreviews-plos-725668748/935964/preview.jpg)
Allelic association results and linkage disequilibrium (LD) plot of the chromosome Xq28 region around the MECP2 gene.
![Genomic map of chromosome X: localization and position of F8 gene and... | Download Scientific Diagram Genomic map of chromosome X: localization and position of F8 gene and... | Download Scientific Diagram](https://www.researchgate.net/publication/301216794/figure/fig1/AS:386670781321217@1469200906987/Genomic-map-of-chromosome-X-localization-and-position-of-F8-gene-and-polymorphic-markers.png)
Genomic map of chromosome X: localization and position of F8 gene and... | Download Scientific Diagram
![PDF] Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region. | Semantic Scholar PDF] Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/071c129d9188362f1840d33129548c2e949c2f37/2-Figure1-1.png)
PDF] Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region. | Semantic Scholar
![Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men](https://www.frontiersin.org/files/MyHome%20Article%20Library/557341/557341_Thumb_400.jpg)
Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men
![Frontiers | Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion Frontiers | Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion](https://www.frontiersin.org/files/Articles/488687/fgene-11-00101-HTML/image_m/fgene-11-00101-g001.jpg)
Frontiers | Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion
![Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/48/12/840/F5.large.jpg)
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics
![The systematic functional characterisation of Xq28 genes prioritises candidate disease genes | BMC Genomics | Full Text The systematic functional characterisation of Xq28 genes prioritises candidate disease genes | BMC Genomics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2F1471-2164-7-29/MediaObjects/12864_2005_Article_412_Fig1_HTML.jpg)
The systematic functional characterisation of Xq28 genes prioritises candidate disease genes | BMC Genomics | Full Text
![Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A](https://genome.cshlp.org/content/15/2/214/F1.large.jpg)
Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A
![Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/48/12/840/F1.large.jpg)
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics
![Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome - Peters - 2019 - Clinical Genetics - Wiley Online Library Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome - Peters - 2019 - Clinical Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5d90a306-6539-4c87-adc4-173e573fabf7/cge13521-toc-0001-m.jpg?trick=1685656518120)
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome - Peters - 2019 - Clinical Genetics - Wiley Online Library
![Activity map of the tammar X chromosome shows that marsupial X inactivation is incomplete and escape is stochastic | Genome Biology | Full Text Activity map of the tammar X chromosome shows that marsupial X inactivation is incomplete and escape is stochastic | Genome Biology | Full Text](https://media.springernature.com/full/springer-static/image/art%3A10.1186%2Fgb-2010-11-12-r122/MediaObjects/13059_2010_Article_2498_Fig2_HTML.jpg)
Activity map of the tammar X chromosome shows that marsupial X inactivation is incomplete and escape is stochastic | Genome Biology | Full Text
![The Relationship between Skewed X-chromosome Inactivation and Neurological Disorders Development | Semantic Scholar The Relationship between Skewed X-chromosome Inactivation and Neurological Disorders Development | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/39a9fb402be3949d397f44d7fe79a60401ec5902/6-Figure5-1.png)