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Q28386577-01C2498B-F701-46EF-972F-7E5C86959267
Q28386577-01C2498B-F701-46EF-972F-7E5C86959267
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http://www.wikidata.org/entity/statement/Q28386577-01C2498B-F701-46EF-972F-7E5C86959267
Expanding the phenotype and genotype of female GnRH deficiency
P2860
Q28386577-01C2498B-F701-46EF-972F-7E5C86959267
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28386577-01C2498B-F701-46EF-972F-7E5C86959267
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681c493e17f4d48f09bb4cd9728cf6cc3bbd3c83
P2860
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.