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Q34752030-2033F7E9-D3A5-4769-BD7C-D08E36BA9477
Q34752030-2033F7E9-D3A5-4769-BD7C-D08E36BA9477
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34752030-2033F7E9-D3A5-4769-BD7C-D08E36BA9477
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.
P921
Q34752030-2033F7E9-D3A5-4769-BD7C-D08E36BA9477
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34752030-2033F7E9-D3A5-4769-BD7C-D08E36BA9477
rank
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type
BestRank
Statement
P921
Kallmann syndrome