Matches in Nanopublications for { ?s ?p "[Although fibroblast growth factor-8 (FGF8) mutations have mainly found in patients with Kallmann syndrome, mice with a hypomorphic Fgf8 allele or complete gene invalidation display, aside from gonadotropin-releasing hormone deficiency, parts or even the entire spectrum of human VATER/VACTERL association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_assertion description "[Although fibroblast growth factor-8 (FGF8) mutations have mainly found in patients with Kallmann syndrome, mice with a hypomorphic Fgf8 allele or complete gene invalidation display, aside from gonadotropin-releasing hormone deficiency, parts or even the entire spectrum of human VATER/VACTERL association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.