Matches in Nanopublications for { ?s ?p "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP2252.RA9Pa5IrXyjLm0mlzaeUScyU5eMsaIT0mM4-etv3lmffo130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2252.RA9Pa5IrXyjLm0mlzaeUScyU5eMsaIT0mM4-etv3lmffo130_provenance.
- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_provenance.
- assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP215509.RAfnnguAQoC3LRMa7w-MEM3P8qwQqgz8LA05v1S9eKJzQ130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215509.RAfnnguAQoC3LRMa7w-MEM3P8qwQqgz8LA05v1S9eKJzQ130_provenance.
- NP4557.RAebDHrbN0hbAcRK-2JM541bz8LVlMLpB8yQWfa9Y-U8Q130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4557.RAebDHrbN0hbAcRK-2JM541bz8LVlMLpB8yQWfa9Y-U8Q130_provenance.
- NP553966.RAqIiSAULJo4sR_HarWhjQJIcLsSBL_7pnm3cZodb-ufs130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553966.RAqIiSAULJo4sR_HarWhjQJIcLsSBL_7pnm3cZodb-ufs130_provenance.
- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.