(Q42595317)

English

Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.

scientific article published on 21 August 2008

Statements

Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1. (English)
21 August 2008

Identifiers

 
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