Matches in Nanopublications for { ?s ?p "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147016.RAJgYh18g8cIPMn5ysKh2rSFP3Amq8esh2tNXfP43gl3Y130_provenance.
- NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152385.RAONjIx_YxVGvh2_FI8WyMhLfLG0lvvxkaG3apWAo2wSc130_provenance.
- NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230560.RAUGrqGqixZby7P1kFjbAuxqRvYBW8twtApgYA_LX-SvA130_provenance.
- NP230559.RAgpNjMvzdkuwI4VJYCziqEMSk9Q0QDjcAWnwJ6Nc80Is130_assertion description "[Homozygous loss-of-function PROK2 mutations cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230559.RAgpNjMvzdkuwI4VJYCziqEMSk9Q0QDjcAWnwJ6Nc80Is130_provenance.