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Q26995332-C8AF5138-6939-4116-BB1B-EF6C84F6A118
Q26995332-C8AF5138-6939-4116-BB1B-EF6C84F6A118
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Statement
http://www.wikidata.org/entity/statement/Q26995332-C8AF5138-6939-4116-BB1B-EF6C84F6A118
Human genetic disorders and knockout mice deficient in glycosaminoglycan
P2860
Q26995332-C8AF5138-6939-4116-BB1B-EF6C84F6A118
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26995332-C8AF5138-6939-4116-BB1B-EF6C84F6A118
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wasDerivedFrom
e3d6259dadfa256df1606de3b91c8b38d117a5bc
P2860
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.