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Q51911649-48579B5F-2C87-4EFA-9259-8FB5272355FE
Q51911649-48579B5F-2C87-4EFA-9259-8FB5272355FE
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http://www.wikidata.org/entity/statement/Q51911649-48579B5F-2C87-4EFA-9259-8FB5272355FE
A maternally inherited chromosome 18q22.1 deletion in a male with late-presenting diaphragmatic hernia and microphthalmia-evaluation of DSEL as a candidate gene for the diaphragmatic defect.
P2860
Q51911649-48579B5F-2C87-4EFA-9259-8FB5272355FE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51911649-48579B5F-2C87-4EFA-9259-8FB5272355FE
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wasDerivedFrom
853d773674c8713730974d81d7788fb4c606db4c
P2860
Congenital diaphragmatic hernia and pulmonary hypoplasia: new insights from developmental biology and genetics