The Relationship between Skewed X-chromosome Inactivation and Neurological Disorders Development
Clinical impacts of genomic copy number gains at Xq28 | Human Genome Variation
Male Homosexuality: Absence of Linkage to Microsatellite Markers at Xq28 | Science
Frontiers | Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion
Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome - Peters - 2019 - Clinical Genetics - Wiley Online Library
XQ28 DUPLICATION INFORMATION
Barth syndrome genetics
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 #
Genes | Free Full-Text | The int22h1/int22h2-Mediated Xq28 Duplication Syndrome: An Intersection between Neurodevelopment, Immunology, and Cancer
Genetic Difference - an overview | ScienceDirect Topics
Do 'gay genes' exist? - GIGAZINE
RPL10 (ribosomal protein L10)
Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review | BMC Medical Genetics | Full Text
The systematic functional characterisation of Xq28 genes prioritises candidate disease genes | BMC Genomics | Full Text
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics
Int22h1/Int22h2‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features - Ballout - 2020 - Human Mutation - Wiley Online Library
The F8 gene; The F8 gene location on the chromosome Xq28 (from... | 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](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")
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
Autist's Corner: Autism-Related Gene Spotlight: MECP2
Polymorphic inversions in chromosome region Xq28 and genomic disorders... | Download Scientific Diagram
Xq28 /MECP2 Duplication and Translocation | MECP2 Duplication Syndrome Blog
Allelic association results and linkage disequilibrium (LD) plot of the chromosome Xq28 region around the MECP2 gene.
![Figure 1. [Facial features of affected males...]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK349624/bin/xq28-dup-Image001.jpg "Figure 1. [Facial features of affected males...]. - GeneReviews® - NCBI Bookshelf")