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17. Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome. Faivre L; Prieur AM; Le Merrer M; Hayem F; Penet C; Woo P; Hofer M; Dagoneau N; Sermet I; Munnich A; Cormier-Daire V Am J Med Genet; 2000 Nov; 95(3):233-6. PubMed ID: 11102929 [TBL] [Abstract][Full Text] [Related]
18. Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome. Nandagopalan RS; Phadke SR; Dalal AB; Ranganath P Indian J Med Res; 2014 Aug; 140(2):221-6. PubMed ID: 25297354 [TBL] [Abstract][Full Text] [Related]
19. A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract. Akawi NA; Ali BR; Al-Gazali L Birth Defects Res A Clin Mol Teratol; 2012 Jul; 94(7):553-6. PubMed ID: 22678705 [TBL] [Abstract][Full Text] [Related]
20. Syndrome of camptodactyly, arthropathy and coxa vara (CAC syndrome). Bahabri S; Sakati N; Hugosson C; Hainau B; Al-Balla SR; Al-Mazyed A; Al-Dalaan A Ann Saudi Med; 1994 Nov; 14(6):479-82. PubMed ID: 17587953 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]