Matches in Nanopublications for { ?s ?p "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- NP168634.RApgKI_hSLH0cukrZCLb4vNj5wkKvN1gyMye7OzSTlU6Q130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168634.RApgKI_hSLH0cukrZCLb4vNj5wkKvN1gyMye7OzSTlU6Q130_provenance.
- NP587107.RA-2qERux3xzwTW9LkCibd1mNf-P9NELZxq4zTktKfPVU130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587107.RA-2qERux3xzwTW9LkCibd1mNf-P9NELZxq4zTktKfPVU130_provenance.
- NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358234.RAPcJghthZWDrsABb4ibFBPnANc0a8Ie7mPBCQ8GDzSIA130_provenance.
- NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400511.RA6zGG_Qj80aCnvJAb9s-LDDMLaOZErskCrUy4RGLuua4130_provenance.
- assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP256654.RA8w6m6lmQvyl_5VcL8nw_i36MgL1tPFyJNM3KXkf-tWQ130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256654.RA8w6m6lmQvyl_5VcL8nw_i36MgL1tPFyJNM3KXkf-tWQ130_provenance.
- NP256655.RAfultQhj_TeAFgEWETWRGniEXvM5bl8UlNusl0298YpY130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256655.RAfultQhj_TeAFgEWETWRGniEXvM5bl8UlNusl0298YpY130_provenance.
- NP400477.RAqtpdJWahIDQDKx84P6jG6lvSAOdpWQJneRhP7-yYMa8130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400477.RAqtpdJWahIDQDKx84P6jG6lvSAOdpWQJneRhP7-yYMa8130_provenance.
- NP256650.RAE4CeIWbqYVaQGuZa-zpkZ_xMQ8WcosVz3kAbuz8kFXE130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256650.RAE4CeIWbqYVaQGuZa-zpkZ_xMQ8WcosVz3kAbuz8kFXE130_provenance.
- NP256652.RAEEUVFvJICnyzaMuggwR-c5nPvsSdaE9gvpIa-c0JRY8130_assertion description "[Pfeiffer syndrome (PS) is one of the classical craniosynostosis syndromes correlated with specific mutations in the human fibroblast growth factor receptor (FGFR) genes, FGFR1 and FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256652.RAEEUVFvJICnyzaMuggwR-c5nPvsSdaE9gvpIa-c0JRY8130_provenance.