Matches in Nanopublications for { ?s ?p "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP120722.RAJ_7jy-3v4ejnAyb6gbvUaYZQgs12YvCXYMFBXyIRWIU130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120722.RAJ_7jy-3v4ejnAyb6gbvUaYZQgs12YvCXYMFBXyIRWIU130_provenance.
- NP153609.RAIC2bQydWT24f3NAdflAcSsBq-grv0-yl5TO-XjvD0Pw130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153609.RAIC2bQydWT24f3NAdflAcSsBq-grv0-yl5TO-XjvD0Pw130_provenance.
- NP183914.RAUBfcK_-nF_X8NLWRaVye57Td2MrDHLR_NXftPbTsrWI130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183914.RAUBfcK_-nF_X8NLWRaVye57Td2MrDHLR_NXftPbTsrWI130_provenance.
- NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193969.RAWCz9Wje7dpHmVHwESj5TBlImpyTh11Dm3wgKSHWfUJg130_provenance.
- NP216716.RAOabupeFteR9ZUXHOVc-xRhuPv-FSwxTvWjxmlYH9pc8130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216716.RAOabupeFteR9ZUXHOVc-xRhuPv-FSwxTvWjxmlYH9pc8130_provenance.
- NP193970.RAKufCbH7u9hQp8-WLKdLpeCcEjRRedICbdFrnNtFvbh8130_assertion description "[Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193970.RAKufCbH7u9hQp8-WLKdLpeCcEjRRedICbdFrnNtFvbh8130_provenance.