These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Multiple epiphyseal dysplasia tarda. A family with autosomal recessive inheritance. Gamboa I; Lisker R Clin Genet; 1974; 6(1):15-9. PubMed ID: 4426126 [No Abstract] [Full Text] [Related]
3. [Poly-epiphyseal dysplasia, probably autosomal recessive. Contribution of the ultrastructural study to the discovery of this autonomous form]. Maroteaux P; Stanescu R; Cohen-Solal D Nouv Presse Med; 1975 Sep; 4(30):2169-72. PubMed ID: 170585 [TBL] [Abstract][Full Text] [Related]
4. Multiple epiphyseal dysplasia. A family case report. Mena HR; Pearson EO JAMA; 1976 Dec; 236(23):2629-33. PubMed ID: 1036536 [TBL] [Abstract][Full Text] [Related]
5. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome. Toriello HV; Higgins JV; Miller T Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015 [TBL] [Abstract][Full Text] [Related]
6. [Two cases of multiple epiphyseal dysplasia with autonomic dysfunction such as hypohidrosis and orthostatic hypotension in a family]. Moritoyo T; Kitajima I; Nakagawa M; Izumo S; Osame M; Igata A Nihon Naika Gakkai Zasshi; 1988 Jul; 77(7):1062-6. PubMed ID: 3235903 [No Abstract] [Full Text] [Related]
7. Epiphyseal dysplasia of the femoral head, severe myopia and perceptive hearing loss in three brothers. Pfeiffer RA; Jünemann G; Polster J; Bauer H Clin Genet; 1973; 4(2):141-4. PubMed ID: 4730943 [No Abstract] [Full Text] [Related]
16. Bilateral failure of the capital femoral epiphysis: bilateral Perthes disease, multiple epiphyseal dysplasia, pseudoachondroplasia, and spondyloepiphyseal dysplasia congenita and tarda. Crossan JF; Wynne-Davies R; Fulford GE J Pediatr Orthop; 1983 Jul; 3(3):297-301. PubMed ID: 6409926 [TBL] [Abstract][Full Text] [Related]
17. [Congenital epiphyseal chondrodysplasia punctata. Study of 9 cases]. Frontera Izquierdo P; Cabezuelo Huerta G; Malo Concepción P An Esp Pediatr; 1985 Sep; 23(3):175-82. PubMed ID: 4073686 [TBL] [Abstract][Full Text] [Related]
18. A CASE OF THE SMITH-LEMLI-OPITZ SYNDROME OF MULTIPLE CONGENITAL ANOMALIES IN ASSOCIATION WITH DYSPLASIA EPIPHYSIALIS PUNCTATA. GIBSON R Can Med Assoc J; 1965 Mar; 92(11):574-5. PubMed ID: 14303408 [No Abstract] [Full Text] [Related]