Matches in Nanopublications for { ?s ?p "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_assertion description "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554671.RA6e6iFamjDczJfrBsOxzn3V4rdoMTw8pW3JShK9btbNk130_provenance.
- assertion description "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_assertion description "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845111.RAJRdtzlE-2GW6JdZr1wNyGt4CkH4sq6IcDiXGtbsQVDQ130_provenance.
- NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_assertion description "[Cutis laxa (CL) is a heterogeneous group of genetic and acquired disorders with at least two autosomal dominant forms caused by mutations in the elastin and fibulin-5 genes, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499363.RAID0fkWHct9fSgdTIbDI31d-AFkfYD9yP_3_Zo4YOErU130_provenance.