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Q24595634-BF2DE4D3-EA40-4910-A136-FC23C4B3D536
Q24595634-BF2DE4D3-EA40-4910-A136-FC23C4B3D536
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24595634-BF2DE4D3-EA40-4910-A136-FC23C4B3D536
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome
P2860
Q24595634-BF2DE4D3-EA40-4910-A136-FC23C4B3D536
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24595634-BF2DE4D3-EA40-4910-A136-FC23C4B3D536
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wasDerivedFrom
dd341a11eaa07aa05ca96a8916e571a6655996bf
P2860
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules