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Q51323089-1C25CDFA-B2B8-46DC-B9AE-F055A0A2D598
Q51323089-1C25CDFA-B2B8-46DC-B9AE-F055A0A2D598
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51323089-1C25CDFA-B2B8-46DC-B9AE-F055A0A2D598
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.
P1433
Q51323089-1C25CDFA-B2B8-46DC-B9AE-F055A0A2D598
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51323089-1C25CDFA-B2B8-46DC-B9AE-F055A0A2D598
rank
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type
BestRank
Statement
wasDerivedFrom
2ec98e845b9420e71732699ba374331d532d12fa
P1433
Pediatric Research