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Q33707256-60D3C4A4-AEF8-445F-BD74-E5F6E402C138
Q33707256-60D3C4A4-AEF8-445F-BD74-E5F6E402C138
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http://www.wikidata.org/entity/statement/Q33707256-60D3C4A4-AEF8-445F-BD74-E5F6E402C138
Phenotypic analysis of Dlx5 overexpression in post-natal bone.
P2860
Q33707256-60D3C4A4-AEF8-445F-BD74-E5F6E402C138
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Statement
http://www.wikidata.org/entity/statement/Q33707256-60D3C4A4-AEF8-445F-BD74-E5F6E402C138
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wasDerivedFrom
99efafdd42c269e322afdff5d1f1e02febe3f8af
P2860
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification