EXTL3
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- Hereditary Multiple Exostoses, Macrocephaly, Congenital Heart
- Gene Ontology Analysis of Arthrogryposis (Multiple Congenital Contractures)
- A Novel 8 Mb Interstitial Deletion of Chromosome 8P12-P21.2
- Chromosome 8P As a Potential Hub for Developmental Neuropsychiatric
- Downloaded CRISPR Screen Gene Summary Data Corrected (Fraser & Plotkin, 2007)
- A Novel Deletion Mutation of the EXT2 Gene in a Large Chinese Pedigree with Hereditary Multiple Exostosis
- Investigating the Influence of Perinatal Nicotine and Alcohol Exposure On
- Atlas Journal
- Unraveling the Molecular Mechanism Underlying ALS-Linked Astrocyte
- Table 10: H. Sapiens Recon 1 Network Confidence Scores and Citations
- 1 Mutations in EXTL3 Cause Neuro-Immuno-Skeletal
- A Statistical Framework for Cross-Tissue Transcriptome-Wide Association Analysis
- The Extostosin Family: Proteins with Many Functions☆
- EXTL3 Mutations Cause Skeletal Dysplasia, Immune Deficiency, and Developmental Delay
- Supplementary Table 1. a Full List of Cancer Genes