File:Robinow syndrome2.jpg
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Summary[edit]
| Description |
English: Autosomal recessive Robinow syndrome. X-ray upper limbs and hands showing mesomelic shortening and brachydactyly (A), gingival hyperplasia (B) and X-ray vertebrae showing hemivertebrae and vertebral fusion. (Limb Malformations & Skeletal Dysplasia Clinic, MSU, NRC). |
| Date | |
| Source | Samia A Temtamy, Mona S Aglan. Brachydactyly. Orphanet Journal of Rare Diseases. 3, 15. 2008. DOI:10.1186/1750-1172-3-15 |
| Author | see above |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 13:08, 4 July 2008 | | 1,200 × 796 (132 KB) | Filip em (talk | contribs) | {{Information |Description={{en|1=Autosomal recessive Robinow syndrome. X-ray upper limbs and hands showing mesomelic shortening and brachydactyly (A), gingival hyperplasia (B) and X-ray vertebrae showing hemivertebrae and vertebral fusion. (Limb Malforma |
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