![Gene structure and organisation in two genomic sequence contigs from... | Download Scientific Diagram Gene structure and organisation in two genomic sequence contigs from... | Download Scientific Diagram](https://www.researchgate.net/publication/14070143/figure/fig2/AS:667587226656772@1536176606539/Gene-structure-and-organisation-in-two-genomic-sequence-contigs-from-Xq28-drawn-to.jpg)
Gene structure and organisation in two genomic sequence contigs from... | Download Scientific Diagram
![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.
![Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy | European Journal of Human Genetics Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy | European Journal of Human Genetics](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fejhg.2008.208/MediaObjects/41431_2009_Article_BFejhg2008208_Fig2_HTML.jpg)
Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy | European Journal of Human Genetics
![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/Articles/557341/fgene-11-557341-HTML-r2/image_m/fgene-11-557341-g001.jpg)
Frontiers | Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men
Simons Searchlight - In the last year we have added 10 genetic conditions to our Simons Searchlight gene list. Look here to see how we've grown: https://bit.ly/32FqduG #RALGAPB #GNB1 #CLCN4 #SCN1B #2q37.3 #
![IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male](https://pub.mdpi-res.com/ijms/ijms-23-01179/article_deploy/html/images/ijms-23-01179-g002.png?1643014884)
IJMS | Free Full-Text | Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male
![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
![Polymorphic inversions in chromosome region Xq28 and genomic disorders... | Download Scientific Diagram Polymorphic inversions in chromosome region Xq28 and genomic disorders... | Download Scientific Diagram](https://www.researchgate.net/publication/341480715/figure/fig2/AS:892823914176519@1589877217403/Polymorphic-inversions-in-chromosome-region-Xq28-and-genomic-disorders-caused-by-other.png)
Polymorphic inversions in chromosome region Xq28 and genomic disorders... | Download Scientific Diagram
![Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males | Genetics in Medicine Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males | Genetics in Medicine](https://media.springernature.com/m685/springer-static/image/art%3A10.1097%2F01.gim.0000250502.28516.3c/MediaObjects/41436_2006_Article_BFgim2006128_Fig3_HTML.jpg)
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males | Genetics in Medicine
![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
![Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia - Lannoy - 2018 - Haemophilia - Wiley Online Library Review of molecular mechanisms at distal Xq28 leading to balanced or unbalanced genomic rearrangements and their phenotypic impacts on hemophilia - Lannoy - 2018 - Haemophilia - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/67768701-b912-43da-a215-37607474f5f6/hae13569-fig-0004-m.jpg)