Ring Chromosome and Clinical Findings: Reports Cases of 4 Different Chromosomes in Beninese Population
A Turner syndrome woman with a ring X chromosome [45,X/46,X,r(X)(p22.3q27)] whose child also had a ring X chromosome
![Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f843cc892703c150b38b7e6ec11e56d3a6ec44a6/3-Figure1-1.png)
Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar
![Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome | SpringerLink Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10815-016-0761-x/MediaObjects/10815_2016_761_Fig1_HTML.gif)
Molecular cytogenetic characterization of two Turner syndrome patients with mosaic ring X chromosome | SpringerLink
![Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0003399504000346-fx3.jpg)
Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect
![Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes](https://www.frontiersin.org/files/Articles/613035/fneur-11-613035-HTML/image_m/fneur-11-613035-t001.jpg)
Frontiers | Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
![Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay | European Journal of Human Genetics Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay | European Journal of Human Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsj.ejhg.5200757/MediaObjects/41431_2002_Article_BF5200757_Fig3_HTML.jpg)
Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay | European Journal of Human Genetics
![PDF] INTERCHROMOSOMAL EFFECTS ON CROSSING-OVER IN DROSOPHILA MELANOGASTER . I . EFFECTS OF COMPOUND AND RING X CHROMOSOMES ON THE THIRD CHROMOSOME 1-2 | Semantic Scholar PDF] INTERCHROMOSOMAL EFFECTS ON CROSSING-OVER IN DROSOPHILA MELANOGASTER . I . EFFECTS OF COMPOUND AND RING X CHROMOSOMES ON THE THIRD CHROMOSOME 1-2 | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/305f228d841bb3dd4bae31a7cd9469ad54f435e8/3-Figure1-1.png)