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Q33861255-3286904B-C2D1-404C-B783-AF9A171CDB16
Q33861255-3286904B-C2D1-404C-B783-AF9A171CDB16
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Statement
http://www.wikidata.org/entity/statement/Q33861255-3286904B-C2D1-404C-B783-AF9A171CDB16
Genetic aspects of human congenital diaphragmatic hernia.
P2860
Q33861255-3286904B-C2D1-404C-B783-AF9A171CDB16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33861255-3286904B-C2D1-404C-B783-AF9A171CDB16
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wasDerivedFrom
66531ca0337a3a6b2605f95b0145a51df1322888
P2860
Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?