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Q51323089-1D883DA5-1412-482F-8062-056AC34A117C
Q51323089-1D883DA5-1412-482F-8062-056AC34A117C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51323089-1D883DA5-1412-482F-8062-056AC34A117C
A novel missense mutation in the transcription factor FOXF1 cosegregating with infantile hypertrophic pyloric stenosis in the extended pedigree linked to IHPS5 on chromosome 16q24.
P2860
Q51323089-1D883DA5-1412-482F-8062-056AC34A117C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51323089-1D883DA5-1412-482F-8062-056AC34A117C
rank
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type
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Statement
wasDerivedFrom
bf142b4c668c0f7676227c80bfbec2c5f01e1f87
P2860
The role of RET genomic variants in infantile hypertrophic pyloric stenosis.