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Q37589830-11C97A84-953A-491F-BF4D-3C496B40A6BB
Q37589830-11C97A84-953A-491F-BF4D-3C496B40A6BB
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http://www.wikidata.org/entity/statement/Q37589830-11C97A84-953A-491F-BF4D-3C496B40A6BB
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
P2860
Q37589830-11C97A84-953A-491F-BF4D-3C496B40A6BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37589830-11C97A84-953A-491F-BF4D-3C496B40A6BB
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wasDerivedFrom
6dd57f62f597dcfb1b1ddbd8855db8b61e6f1a08
P2860
Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus.