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Q56266779-0D02796D-C7E0-4719-905E-64FFF06BD9C6
Q56266779-0D02796D-C7E0-4719-905E-64FFF06BD9C6
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Statement
http://www.wikidata.org/entity/statement/Q56266779-0D02796D-C7E0-4719-905E-64FFF06BD9C6
Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome
P2860
Q56266779-0D02796D-C7E0-4719-905E-64FFF06BD9C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q56266779-0D02796D-C7E0-4719-905E-64FFF06BD9C6
rank
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type
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wasDerivedFrom
de98419a2751af30470f545b40ffa2379995957c
P2860
Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting