t/gene-ext2

EXT2 gene

Discuss publications and research concerning the EXT2 gene.

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Related literature

High-coverage paleo-genome research identifies a pathogenic mutation on EXT1 in a Qing-period Chinese individual with multiple osteochondromas.
EXT2
Neuropsychiatric Phenotype in a Patient with Neurodevelopmental Disorder with or Without Early-Onset Generalized Epilepsy (NEDEGE).
EXT2
Hereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments.
EXT2
[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses].
EXT2
Genetic alterations in chondrosarcomas - keys to targeted therapies?
EXT2
Mutation analysis and prenatal diagnosis of EXT1 gene mutations in Chinese patients with multiple osteochondromas.
EXT2
Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients.
EXT2
Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).
EXT2
Three novel EXT1 and EXT2 gene mutations in Taiwanese patients with multiple exostoses.
EXT2
[A mutation 1633-26(C-->A) in EXT1 gene causes multiple exostoses].
EXT2

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