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Novel Fgfr1 Mutations in Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: Evidence for the Involvement of an Alternatively Spliced Isoform

AuthID
P-00G-VNR

Author(s)

Gonçalves, C

Bastos, M

Pignatelli, D

Borges, T

Aragüés, JM

Fonseca, F

Pereira, BD

Socorro, S

Lemos, MC

Tipo de Documento

Article

Year published

2015

Publicado

in Fertility and Sterility, ISSN: 0015-0282

Volume: 104, Número: 5, Páginas: 1261-1267.e1

Indexing

Scopus^®

Crossref^®16

Google Scholar^®

Publication Identifiers

DOI: 10.1016/j.fertnstert.2015.07.1142

SCOPUS: 2-s2.0-84946480832

Source Identifiers

ISSN: 0015-0282

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Novel Fgfr1 Mutations in Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: Evidence for the Involvement of an Alternatively Spliced Isoform

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Novel Fgfr1 Mutations in Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism: Evidence for the Involvement of an Alternatively Spliced Isoform

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