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Q51911649-E0D42785-61EB-40EC-AC88-95EEAB26F49C
Q51911649-E0D42785-61EB-40EC-AC88-95EEAB26F49C
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http://www.wikidata.org/entity/statement/Q51911649-E0D42785-61EB-40EC-AC88-95EEAB26F49C
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-E0D42785-61EB-40EC-AC88-95EEAB26F49C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51911649-E0D42785-61EB-40EC-AC88-95EEAB26F49C
rank
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wasDerivedFrom
853d773674c8713730974d81d7788fb4c606db4c
P2860
Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.