| scholarly article | Q13442814 |
| P356 | DOI | 10.1089/GTMB.2010.0040 |
| P698 | PubMed publication ID | 21039224 |
| P2093 | author name string | Yan Zhou | |
| Bin Hu | |||
| Dongsheng Huang | |||
| Yiming Wang | |||
| Weijun Huang | |||
| Peiqiang Su | |||
| Yuanyuan Pei | |||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 865-872 | |
| P577 | publication date | 2010-11-01 | |
| P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
| P1476 | title | Novel mutations of EXT1 and EXT2 genes among families and sporadic cases with multiple exostoses | |
| P478 | volume | 14 |
| Q37342783 | Bilateral Scapulothoracic Osteochondromas in a Patient With Hereditary Multiple Exostosis: A Case Report and Review of the Literature |
| Q44366836 | Clinical characteristics of hereditary multiple exostoses: a retrospective study of mainland chinese cases in recent 23 years |
| Q52346538 | Current paediatric orthopaedic practice in hereditary multiple osteochondromas of the forearm: a systematic review. |
| Q44257198 | Novel and recurrent mutations in the EXT1 and EXT2 genes in Chinese kindreds with multiple osteochondromas |
| Q64264987 | RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas |
Search more.