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Q47971287-D29615F3-9797-4E5F-8E0C-2ED2C74B933E
Q47971287-D29615F3-9797-4E5F-8E0C-2ED2C74B933E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47971287-D29615F3-9797-4E5F-8E0C-2ED2C74B933E
Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosis.
P304
Q47971287-D29615F3-9797-4E5F-8E0C-2ED2C74B933E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47971287-D29615F3-9797-4E5F-8E0C-2ED2C74B933E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ab5f00424b8d401229f8bfa3aa2ade77cb3da149
P304
559-563
http://www.w3.org/2001/XMLSchema#string