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Q55076940-D0A09C1F-7962-4B4B-886E-B587055831A2
Q55076940-D0A09C1F-7962-4B4B-886E-B587055831A2
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http://www.wikidata.org/entity/statement/Q55076940-D0A09C1F-7962-4B4B-886E-B587055831A2
Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria.
P2860
Q55076940-D0A09C1F-7962-4B4B-886E-B587055831A2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55076940-D0A09C1F-7962-4B4B-886E-B587055831A2
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wasDerivedFrom
3794ef9f27f3d540782db14d0c717944de8c4f3d
P2860
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.