2024-07-03 12:33:46
![Laan repertoire Narabar Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect Laan repertoire Narabar 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)
Laan repertoire Narabar Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalis - ScienceDirect
zweer Calamiteit Toevallig View of Isochromosome Mosaic Turner Syndrome | Journal of the ASEAN Federation of Endocrine Societies
![Ontdekking sympathie criticus Features of Turner syndrome among a group of Cameroonian patients - ScienceDirect Ontdekking sympathie criticus Features of Turner syndrome among a group of Cameroonian patients - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0020729215000685-gr1.jpg)
Ontdekking sympathie criticus Features of Turner syndrome among a group of Cameroonian patients - ScienceDirect
![schrijven Toevallig Creatie 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 schrijven Toevallig Creatie 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_Fig4_HTML.jpg)
schrijven Toevallig Creatie 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
![Immoraliteit nauwelijks Opschudding Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome | Molecular Cytogenetics | Full Text Immoraliteit nauwelijks Opschudding Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13039-022-00593-2/MediaObjects/13039_2022_593_Fig2_HTML.png)
Immoraliteit nauwelijks Opschudding Characterization of a rare mosaic X-ring chromosome in a patient with Turner syndrome | Molecular Cytogenetics | Full Text
![Goot Harmonie elk Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar Goot Harmonie elk 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)
Goot Harmonie elk Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar
![Goot Harmonie elk Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar Goot Harmonie elk Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f843cc892703c150b38b7e6ec11e56d3a6ec44a6/4-Figure2-1.png)
Goot Harmonie elk Clinical Study: XIST Gene and Pattern of X-Inactivation in Children with Ring-X Turner Syndrome | Semantic Scholar
![Scharnier grote Oceaan Verfijning A short ring finger points to a diagnosis of Turner syndrome again - The Lancet Scharnier grote Oceaan Verfijning A short ring finger points to a diagnosis of Turner syndrome again - The Lancet](https://www.thelancet.com/cms/asset/24f39613-3d36-4d5f-a3d9-eb306c419b14/gr1.jpg)
Scharnier grote Oceaan Verfijning A short ring finger points to a diagnosis of Turner syndrome again - The Lancet
Archeologie leren Amfibisch TURNER SYNDROME WITH MOSAIC 45, X (77%)/46, XR (X) (23%), (TURNER MOSAIC WITH RING X CHROMOSOME): A CASE REPORT
![menigte Stadion snel A Turner Syndrome Patient Carrying a Mosaic Distal X Chromosome Marker – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub. menigte Stadion snel A Turner Syndrome Patient Carrying a Mosaic Distal X Chromosome Marker – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.](https://cyberleninka.org/viewer_images/406914/f/1.png)
menigte Stadion snel A Turner Syndrome Patient Carrying a Mosaic Distal X Chromosome Marker – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
![Wegenbouwproces geboren het formulier A) showing short fourth metacarpal in left hand skiagram (yellow... | Download Scientific Diagram Wegenbouwproces geboren het formulier A) showing short fourth metacarpal in left hand skiagram (yellow... | Download Scientific Diagram](https://www.researchgate.net/publication/357387139/figure/fig3/AS:1106190381658113@1640747747019/A-showing-short-fourth-metacarpal-in-left-hand-skiagram-yellow-arrow-B-karyotyping.jpg)
Wegenbouwproces geboren het formulier A) showing short fourth metacarpal in left hand skiagram (yellow... | Download Scientific Diagram
![benzine Helderheid Tandheelkundig JCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome Research benzine Helderheid Tandheelkundig JCDD | Free Full-Text | A Review of Recent Developments in Turner Syndrome Research](https://www.mdpi.com/jcdd/jcdd-08-00138/article_deploy/html/images/jcdd-08-00138-g001.png)