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Q33654193-13024B66-1B02-428D-BD8D-850835E17801
Q33654193-13024B66-1B02-428D-BD8D-850835E17801
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http://www.wikidata.org/entity/statement/Q33654193-13024B66-1B02-428D-BD8D-850835E17801
Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.
P2860
Q33654193-13024B66-1B02-428D-BD8D-850835E17801
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33654193-13024B66-1B02-428D-BD8D-850835E17801
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wasDerivedFrom
9a4d7172461e69535b6ee6f404aeb69edbb443ab
P2860
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome