Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review | BMC Medical Genetics | Full Text
![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")
Figure 1. [Facial features of affected males...]. - GeneReviews® - NCBI Bookshelf
Infectious and Immunologic Phenotype of MECP2 Duplication Syndrome | SpringerLink
Frontiers | Skewed X-Chromosome Inactivation and Compensatory Upregulation of Escape Genes Precludes Major Clinical Symptoms in a Female With a Large Xq Deletion
Allelic association results and linkage disequilibrium (LD) plot of the chromosome Xq28 region around the MECP2 gene.
Genes | Free Full-Text | The int22h1/int22h2-Mediated Xq28 Duplication Syndrome: An Intersection between Neurodevelopment, Immunology, and Cancer
Clinical impacts of genomic copy number gains at Xq28 | Human Genome Variation
Barth syndrome genetics
Unreleased Xq28 Gene Study Repeats Unproven Theory - Voice of the Voiceless
Genetics and classification of hemophilia | Contemporary Approaches to Hemophilia
Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions | Journal of Medical Genetics
File:ABCD1-gene.svg - Wikimedia Commons
X-linked clinical anophthalmos Localization of the gene to Xq27-Xq28: Ophthalmic Paediatrics and Genetics: Vol 12, No 1
The Relationship between Skewed X-chromosome Inactivation and Neurological Disorders Development
Xq28 - Wikipedia
Polymorphic inversions in chromosome region Xq28 and genomic disorders... | Download Scientific Diagram
Genetic Difference - an overview | ScienceDirect Topics
The F8 gene; The F8 gene location on the chromosome Xq28 (from... | Download Scientific Diagram
Male Homosexuality: Absence of Linkage to Microsatellite Markers at Xq28 | Science
group_3_presentation_3_-_biological_basis_of_sexuality - Wiki
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
