Matches in Nanopublications for { ?s ?p "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP838651.RAZs51f47qdbypv2POCbSXupa4KRUHV36t1kGawd3YrRI130_assertion description "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838651.RAZs51f47qdbypv2POCbSXupa4KRUHV36t1kGawd3YrRI130_provenance.
- NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_assertion description "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939776.RAZLvm2Y-XAXVBiJXqoKOPBkY1PBHyZV0_0AU3jShEea8130_provenance.
- assertion description "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP988255.RAYa5uG5YJ6nsbyjUNDM5CWPhmMsf96S6dbm3kq8EJtUQ130_assertion description "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988255.RAYa5uG5YJ6nsbyjUNDM5CWPhmMsf96S6dbm3kq8EJtUQ130_provenance.
- NP988254.RAgA_nPHaA6syFQ-EgypAwTo0r3AjOZcbplP12b5vB_Gc130_assertion description "[A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988254.RAgA_nPHaA6syFQ-EgypAwTo0r3AjOZcbplP12b5vB_Gc130_provenance.