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Q38794125-3A2524C8-B287-4440-85F7-D8FDF7F27FAF
Q38794125-3A2524C8-B287-4440-85F7-D8FDF7F27FAF
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Statement
http://www.wikidata.org/entity/statement/Q38794125-3A2524C8-B287-4440-85F7-D8FDF7F27FAF
Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.
P2860
Q38794125-3A2524C8-B287-4440-85F7-D8FDF7F27FAF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38794125-3A2524C8-B287-4440-85F7-D8FDF7F27FAF
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wasDerivedFrom
ccab05a3b6788265a425476d7eecfbc8dbb64acc
P2860
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome.