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Q37718486-1C476C0C-D7EA-4D65-B50F-850E8F8B5D71
Q37718486-1C476C0C-D7EA-4D65-B50F-850E8F8B5D71
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http://www.wikidata.org/entity/statement/Q37718486-1C476C0C-D7EA-4D65-B50F-850E8F8B5D71
Whole exome sequencing in a patient with uniparental disomy of chromosome 2 and a complex phenotype.
P2860
Q37718486-1C476C0C-D7EA-4D65-B50F-850E8F8B5D71
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37718486-1C476C0C-D7EA-4D65-B50F-850E8F8B5D71
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type
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wasDerivedFrom
ac71e4d34ef6d43b97341f0ee0ab9f2827d60e57
P2860
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes