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Q35678026-FAAC0B10-F077-476D-92A7-E6B30D2905B2
Q35678026-FAAC0B10-F077-476D-92A7-E6B30D2905B2
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Statement
http://www.wikidata.org/entity/statement/Q35678026-FAAC0B10-F077-476D-92A7-E6B30D2905B2
A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder.
P2860
Q35678026-FAAC0B10-F077-476D-92A7-E6B30D2905B2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35678026-FAAC0B10-F077-476D-92A7-E6B30D2905B2
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wasDerivedFrom
b3bc915647c2c447e95026f0f13363f4128ccf15
P2860
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.