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Q47147634-08C1291A-0277-4306-BAF4-DEFF3AA0C601
Q47147634-08C1291A-0277-4306-BAF4-DEFF3AA0C601
BestRank
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http://www.wikidata.org/entity/statement/Q47147634-08C1291A-0277-4306-BAF4-DEFF3AA0C601
Genes uniquely expressed in human growth plate chondrocytes uncover a distinct regulatory network.
P2860
Q47147634-08C1291A-0277-4306-BAF4-DEFF3AA0C601
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47147634-08C1291A-0277-4306-BAF4-DEFF3AA0C601
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wasDerivedFrom
f2dec1aaa1a74d0a04f47f226a65de9541a8f684
P2860
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.