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Hereditary multiple osteochondromas in Jordanian patients: Mutational and immunohistochemical analysis of <em>EXT1</em> and <em>EXT2</em> genes
![The EXT proteins and HS biosynthesis. (a) Schematic representations of... | Download Scientific Diagram The EXT proteins and HS biosynthesis. (a) Schematic representations of... | Download Scientific Diagram](https://www.researchgate.net/publication/11826439/figure/fig1/AS:667210615889927@1536086815597/The-EXT-proteins-and-HS-biosynthesis-a-Schematic-representations-of-the-EXT1-and-EXT2.png)
The EXT proteins and HS biosynthesis. (a) Schematic representations of... | Download Scientific Diagram
![Medicina | Free Full-Text | Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family Medicina | Free Full-Text | Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family](https://www.mdpi.com/medicina/medicina-59-00100/article_deploy/html/images/medicina-59-00100-g001.png)
Medicina | Free Full-Text | Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family
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Structural basis for heparan sulfate co-polymerase action by the EXT1–2 complex | Nature Chemical Biology
![A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG | Scientific Reports A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep06407/MediaObjects/41598_2014_Article_BFsrep06407_Fig1_HTML.jpg)
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG | Scientific Reports
![Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing](https://www.spandidos-publications.com/article_images/mmr/15/2/MMR-15-02-0657-g03.jpg)
Identification of a novel mutation in the EXT1 gene from a patient with multiple osteochondromas by exome sequencing
![Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene | Molecular Cytogenetics | Full Text Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene | Molecular Cytogenetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13039-023-00638-0/MediaObjects/13039_2023_638_Fig4_HTML.png)
Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene | Molecular Cytogenetics | Full Text
![Frontiers | EXT1 and EXT2 Variants in 22 Chinese Families With Multiple Osteochondromas: Seven New Variants and Potentiation of Preimplantation Genetic Testing and Prenatal Diagnosis Frontiers | EXT1 and EXT2 Variants in 22 Chinese Families With Multiple Osteochondromas: Seven New Variants and Potentiation of Preimplantation Genetic Testing and Prenatal Diagnosis](https://www.frontiersin.org/files/Articles/607838/fgene-11-607838-HTML/image_m/fgene-11-607838-g004.jpg)
Frontiers | EXT1 and EXT2 Variants in 22 Chinese Families With Multiple Osteochondromas: Seven New Variants and Potentiation of Preimplantation Genetic Testing and Prenatal Diagnosis
![Sweet news : 3D structure reveals mechanism of heparan sulfate chain polymerization - IBS - Institut de Biologie Structurale - Grenoble / France Sweet news : 3D structure reveals mechanism of heparan sulfate chain polymerization - IBS - Institut de Biologie Structurale - Grenoble / France](https://www.ibs.fr/IMG/jpg/illustration_naturecom_2022_11_wild.jpg)
Sweet news : 3D structure reveals mechanism of heparan sulfate chain polymerization - IBS - Institut de Biologie Structurale - Grenoble / France
Exome Sequencing and Functional Analysis Identifies a Novel Mutation in EXT1 Gene That Causes Multiple Osteochondromas | PLOS ONE
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