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1
Q48892428-36DFB0CC-51C6-498E-B99F-30E81C3730B4
Q48892428-36DFB0CC-51C6-498E-B99F-30E81C3730B4
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Statement
http://www.wikidata.org/entity/statement/Q48892428-36DFB0CC-51C6-498E-B99F-30E81C3730B4
CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
P2860
Q48892428-36DFB0CC-51C6-498E-B99F-30E81C3730B4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48892428-36DFB0CC-51C6-498E-B99F-30E81C3730B4
rank
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type
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Statement
wasDerivedFrom
ebb6da2501fe2341d72f96551d93735581722bce
P2860
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations