Novel Fgfr1 Mutations in Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: Evidence for the Involvement of an Alternatively Spliced Isoform
                        AuthID
P-00G-VNR
                
    P-00G-VNR
© 2025 CRACS & Inesc TEC - All Rights Reserved Privacy Policy | Terms of Service