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Q34752030-300D7BEC-07F9-4FEC-855B-EBAFF98410DD
Q34752030-300D7BEC-07F9-4FEC-855B-EBAFF98410DD
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http://www.wikidata.org/entity/statement/Q34752030-300D7BEC-07F9-4FEC-855B-EBAFF98410DD
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.
P2860
Q34752030-300D7BEC-07F9-4FEC-855B-EBAFF98410DD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34752030-300D7BEC-07F9-4FEC-855B-EBAFF98410DD
rank
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type
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Statement
wasDerivedFrom
5657c9c46b9b4fe1534110fda2f0e861a9f400c8
P2860
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome