Matches in Nanopublications for { ?s ?p "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369855.RA4ZvJe0As7TBr9xTF3lyAOTP5AuvsOPGff90ga2dOdEQ130_provenance.
- NP542732.RA1jrX5DBNMa004plCLMmdH6zPqnATT5timr1HwglvE6E130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542732.RA1jrX5DBNMa004plCLMmdH6zPqnATT5timr1HwglvE6E130_provenance.
- assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400906.RAYwnZfvYEXgopMsQSk8dWlX68TYHq-HPL3MplNwKfNos130_provenance.
- NP401257.RAbZJMTmQ8vZ7OyG_irm3e6SyiQcwvdK-Nf8kboYyLa_Q130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401257.RAbZJMTmQ8vZ7OyG_irm3e6SyiQcwvdK-Nf8kboYyLa_Q130_provenance.
- NP1049788.RA3BNAtMYwiVb7RgNr8u7i43iRwnl4d1Th0Aiwv0vJEAc130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049788.RA3BNAtMYwiVb7RgNr8u7i43iRwnl4d1Th0Aiwv0vJEAc130_provenance.
- NP1049789.RA05R391_-dIT3hdgMRzdOxtmCLtPIapiCzeP3VmVod-M130_assertion description "[Muenke syndrome is an autosomal dominant craniosynostosis syndrome resulting from a defining point mutation in the Fibroblast Growth Factor Receptor3 (FGFR3) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049789.RA05R391_-dIT3hdgMRzdOxtmCLtPIapiCzeP3VmVod-M130_provenance.