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Q41771489-E214BF1B-460D-4C5C-BFCF-B1051417E78B
Q41771489-E214BF1B-460D-4C5C-BFCF-B1051417E78B
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http://www.wikidata.org/entity/statement/Q41771489-E214BF1B-460D-4C5C-BFCF-B1051417E78B
Clinical utility gene card for: Meckel syndrome - update 2016.
P2860
Q41771489-E214BF1B-460D-4C5C-BFCF-B1051417E78B
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Statement
http://www.wikidata.org/entity/statement/Q41771489-E214BF1B-460D-4C5C-BFCF-B1051417E78B
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wasDerivedFrom
a2b60c91b766f850148b57f022fb9b1bfc6c8d73
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.