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Q38681476-BCCB2CF9-9059-41F7-899E-05979FFFB1FA
Q38681476-BCCB2CF9-9059-41F7-899E-05979FFFB1FA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38681476-BCCB2CF9-9059-41F7-899E-05979FFFB1FA
Expanding the mutation and clinical spectrum of Roberts syndrome.
P2860
Q38681476-BCCB2CF9-9059-41F7-899E-05979FFFB1FA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38681476-BCCB2CF9-9059-41F7-899E-05979FFFB1FA
rank
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Statement
wasDerivedFrom
7884bc0bc8e368171e7cfafd3ba6f13ec3b6c427
P2860
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.