Matches in Nanopublications for { ?s ?p "[Prior to the recent characterization of the enzymatic defect and identification of the involved gene, the histopathology of X-linked dominant chondrodysplasia punctata (Conradi-H�nermann-Happle syndrome or CDPX2) has been described under various names including calcinosis universalis, chondrodystrophia calcificans congenita, Conradi disease, and Conradi-H�nermann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP505622.RAqNXatmM_4nffS17kWtVydo-6iZ6VAUgCLhjDV_soPGM130_assertion description "[Prior to the recent characterization of the enzymatic defect and identification of the involved gene, the histopathology of X-linked dominant chondrodysplasia punctata (Conradi-H�nermann-Happle syndrome or CDPX2) has been described under various names including calcinosis universalis, chondrodystrophia calcificans congenita, Conradi disease, and Conradi-H�nermann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505622.RAqNXatmM_4nffS17kWtVydo-6iZ6VAUgCLhjDV_soPGM130_provenance.
- NP593377.RAG6dv0o28zeXJA-tyCW4EwoFJhF85KKio49hl2TbBlRY130_assertion description "[Prior to the recent characterization of the enzymatic defect and identification of the involved gene, the histopathology of X-linked dominant chondrodysplasia punctata (Conradi-H�nermann-Happle syndrome or CDPX2) has been described under various names including calcinosis universalis, chondrodystrophia calcificans congenita, Conradi disease, and Conradi-H�nermann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593377.RAG6dv0o28zeXJA-tyCW4EwoFJhF85KKio49hl2TbBlRY130_provenance.
- NP428282.RABUOxBa2PLQ2ajjPgove_RjkvG_TOKDZFDd1OZbxS02o130_assertion description "[Prior to the recent characterization of the enzymatic defect and identification of the involved gene, the histopathology of X-linked dominant chondrodysplasia punctata (Conradi-H�nermann-Happle syndrome or CDPX2) has been described under various names including calcinosis universalis, chondrodystrophia calcificans congenita, Conradi disease, and Conradi-H�nermann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428282.RABUOxBa2PLQ2ajjPgove_RjkvG_TOKDZFDd1OZbxS02o130_provenance.