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43. Arachidonic acid metabolism in fibroblasts from patients with peroxisomal diseases: response to interleukin 1. Tiffany CW; Hoefler S; Moser HW; Burch RM Biochim Biophys Acta; 1990 Nov; 1096(1):41-6. PubMed ID: 2125233 [TBL] [Abstract][Full Text] [Related]
44. A lethal skeletal dysplasia with features of chondrodysplasia punctata and osteogenesis imperfecta: an example of Astley-Kendall dysplasia. Further delineation of a rare genetic disorder. Elçioglu N; Hall CM J Med Genet; 1998 Jun; 35(6):505-7. PubMed ID: 9643294 [TBL] [Abstract][Full Text] [Related]
45. Chondrodystrophia calcificans congenita. Report of a case and review of the literature. JOSEPHSON BM; ORIATTI MD Pediatrics; 1961 Sep; 28():425-35. PubMed ID: 13790764 [No Abstract] [Full Text] [Related]
46. Dysplasia epiphysialis punctata; report of a case and review of literature. FRANK WW; DENNY MG J Bone Joint Surg Br; 1954 Feb; 36-B(1):118-22. PubMed ID: 13130633 [No Abstract] [Full Text] [Related]
47. [Osteogenesis imperfecta cystica (Fairbank)--a special form of osteogenesis imperfecta congenita (Vrolik) (author's transl)]. Clemens D; Benz HJ Rofo; 1979 Jul; 131(1):72-7. PubMed ID: 157936 [TBL] [Abstract][Full Text] [Related]
48. [Poly-epiphysial dysplasia with extensive involvement of the spine. Apropos of a case polyepiphysial dysplasia comparable, in some characteristics, to Norquio's disease (fifth type of polyepiphysial dysplasia?]. Berio A; Quazza GF Minerva Pediatr; 1966 Nov; 18(36):2111-8. PubMed ID: 4968630 [No Abstract] [Full Text] [Related]
49. [Chondrodystrophia calcificans congenita in an infant]. Horanský V Cesk Pediatr; 1965 Sep; 20(9):798-9. PubMed ID: 5851907 [No Abstract] [Full Text] [Related]
50. [OSTEOGENESIS IMPERFECTA]. NIELSEN B Nord Med; 1965 Mar; 73():260-3. PubMed ID: 14259633 [No Abstract] [Full Text] [Related]
51. Maxillonasal dysplasia (Binder's syndrome) and chondrodysplasia punctata. Serville F J Med Genet; 1992 Feb; 29(2):141. PubMed ID: 1613767 [No Abstract] [Full Text] [Related]