Matches in Nanopublications for { ?s ?p "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP453761.RAAlxXTooqZ-1swxEIW13KIzV7DT3cArCOmWD29baemXY130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453761.RAAlxXTooqZ-1swxEIW13KIzV7DT3cArCOmWD29baemXY130_provenance.
- NP453763.RABBqLGlyNkQ6S_XCIwufU8280_IUXHw1bQjRRmn9OlA4130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453763.RABBqLGlyNkQ6S_XCIwufU8280_IUXHw1bQjRRmn9OlA4130_provenance.
- NP453764.RACWVP9XJYv-uiVHiHUnsh0i-Fil6NoAQz1cd0pUEa6QI130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453764.RACWVP9XJYv-uiVHiHUnsh0i-Fil6NoAQz1cd0pUEa6QI130_provenance.
- assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP453762.RA31lDFQ36iH3n-0TXpzuWW9R39BZzU04x9W0TvNDrtoE130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453762.RA31lDFQ36iH3n-0TXpzuWW9R39BZzU04x9W0TvNDrtoE130_provenance.
- NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401638.RAFCm5SnooFgrtVp9Zm5B1lvaF2IWEs_70XJHMJzGqmbc130_provenance.
- NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401669.RAH9yT1W_W6rGVdAqK2mOIHrdDNSNHJu1JFtjRdq3pppU130_provenance.
- NP453760.RAeqwBcC1dy7Nt6f7wA6QqO0Hy42h1WfidCAjwT2Bw9mA130_assertion description "[Gain-of-function missense mutations in FGF receptor 2 (FGFR2) are responsible for a variety of craniosynostosis syndromes including Apert syndrome (AS), Pfeiffer syndrome (PS) and Crouzon syndrome (CS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453760.RAeqwBcC1dy7Nt6f7wA6QqO0Hy42h1WfidCAjwT2Bw9mA130_provenance.