Matches in Nanopublications for { ?s ?p "[Other mutations within the FGFR3 tyrosine kinase domain (e.g., C1620A or C1620G [both resulting in Asn540Lys]) are known to cause hypochondroplasia, a relatively common but milder skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_assertion description "[Other mutations within the FGFR3 tyrosine kinase domain (e.g., C1620A or C1620G [both resulting in Asn540Lys]) are known to cause hypochondroplasia, a relatively common but milder skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927886.RAu7c43A7FJYXvKUSBqbcURCkbHeXZdKmzkTyYZ9sNsqA130_provenance.
- NP265007.RA4I5PgPH4a2a7i6N0T0z16ftvlfH3peOEZK4EruTVX2A130_assertion description "[Other mutations within the FGFR3 tyrosine kinase domain (e.g., C1620A or C1620G [both resulting in Asn540Lys]) are known to cause hypochondroplasia, a relatively common but milder skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265007.RA4I5PgPH4a2a7i6N0T0z16ftvlfH3peOEZK4EruTVX2A130_provenance.
- assertion description "[Other mutations within the FGFR3 tyrosine kinase domain (e.g., C1620A or C1620G [both resulting in Asn540Lys]) are known to cause hypochondroplasia, a relatively common but milder skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP298860.RANjgS9sYJIDY-Rmoiyo8UreeFoxxNbuMnJqY1y8NxTeU130_assertion description "[Other mutations within the FGFR3 tyrosine kinase domain (e.g., C1620A or C1620G [both resulting in Asn540Lys]) are known to cause hypochondroplasia, a relatively common but milder skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298860.RANjgS9sYJIDY-Rmoiyo8UreeFoxxNbuMnJqY1y8NxTeU130_provenance.