Matches in Nanopublications for { ?s ?p "[In addition, the p.P252R mutation in FGFR1 was detected in 1 PS patient with unilateral coronal craniosynostosis expanding the phenotypic spectrum of PS with this particular mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP604014.RApftMXEsVO3QX3kL4C6F1tD9tGCUt_BwzCawoVuciLTk130_assertion description "[In addition, the p.P252R mutation in FGFR1 was detected in 1 PS patient with unilateral coronal craniosynostosis expanding the phenotypic spectrum of PS with this particular mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP604014.RApftMXEsVO3QX3kL4C6F1tD9tGCUt_BwzCawoVuciLTk130_provenance.
- NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_assertion description "[In addition, the p.P252R mutation in FGFR1 was detected in 1 PS patient with unilateral coronal craniosynostosis expanding the phenotypic spectrum of PS with this particular mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1046692.RAbzaPtQx_r7Ilj3508NGXmQKGtbaaz2HwawSDDPLVnJY130_provenance.
- NP400254.RAHrG7_D2rarvlgtXC0H4_Ihs4arRSt7TLYhSeowRY3QE130_assertion description "[In addition, the p.P252R mutation in FGFR1 was detected in 1 PS patient with unilateral coronal craniosynostosis expanding the phenotypic spectrum of PS with this particular mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400254.RAHrG7_D2rarvlgtXC0H4_Ihs4arRSt7TLYhSeowRY3QE130_provenance.