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Q36648083-8C8501BE-7D2A-4B1D-A298-C6FCAF87C60D
Q36648083-8C8501BE-7D2A-4B1D-A298-C6FCAF87C60D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36648083-8C8501BE-7D2A-4B1D-A298-C6FCAF87C60D
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS.
P2860
Q36648083-8C8501BE-7D2A-4B1D-A298-C6FCAF87C60D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36648083-8C8501BE-7D2A-4B1D-A298-C6FCAF87C60D
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type
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wasDerivedFrom
4af72e26338b7fd64d544538651558d7bd76754a
P2860
Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers.