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Q35752792-2ECCD863-FDF4-49A8-B33D-E97F3AB15BA8
Q35752792-2ECCD863-FDF4-49A8-B33D-E97F3AB15BA8
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http://www.wikidata.org/entity/statement/Q35752792-2ECCD863-FDF4-49A8-B33D-E97F3AB15BA8
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
P2860
Q35752792-2ECCD863-FDF4-49A8-B33D-E97F3AB15BA8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35752792-2ECCD863-FDF4-49A8-B33D-E97F3AB15BA8
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wasDerivedFrom
43fce5ba2466ac5765f9e51e59d9b8207c757fb4
P2860
Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients