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Q41918641-37F75822-6FB2-4EB5-A410-10E9BC385F6B
Q41918641-37F75822-6FB2-4EB5-A410-10E9BC385F6B
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http://www.wikidata.org/entity/statement/Q41918641-37F75822-6FB2-4EB5-A410-10E9BC385F6B
Clinical utility gene card for: Meckel syndrome.
P2860
Q41918641-37F75822-6FB2-4EB5-A410-10E9BC385F6B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41918641-37F75822-6FB2-4EB5-A410-10E9BC385F6B
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wasDerivedFrom
c949956e4178f6b826e63443b662d6dbabbf9d53
P2860
Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies.