Matches in Nanopublications for { ?s ?p "[We now report a Cx26 mutation in three families with mutilating keratoderma and deafness [Vohwinkel's syndrome (VS; MIM 124500), as originally described].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We now report a Cx26 mutation in three families with mutilating keratoderma and deafness [Vohwinkel's syndrome (VS; MIM 124500), as originally described].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We now report a Cx26 mutation in three families with mutilating keratoderma and deafness [Vohwinkel's syndrome (VS; MIM 124500), as originally described].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP426441.RATp9uSZhfyPXgqF1cwfCJPartLfnQ0j1vlFWXHU4OCtk130_assertion description "[We now report a Cx26 mutation in three families with mutilating keratoderma and deafness [Vohwinkel's syndrome (VS; MIM 124500), as originally described].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426441.RATp9uSZhfyPXgqF1cwfCJPartLfnQ0j1vlFWXHU4OCtk130_provenance.
- NP255127.RABSleXe5ZZiVs1cLmnzw7lqxKaK7_EVH4cX1oeGfKjSQ130_assertion description "[We now report a Cx26 mutation in three families with mutilating keratoderma and deafness [Vohwinkel's syndrome (VS; MIM 124500), as originally described].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255127.RABSleXe5ZZiVs1cLmnzw7lqxKaK7_EVH4cX1oeGfKjSQ130_provenance.