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.
49. [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]
50. Serum lipid analysis confirms the diagnosis of X-linked dominant chondrodysplasia punctata - Conradi-Hünermann-Happle syndrome. Lindenthal B; Repgen R; Emons D; Lentze MJ; von Bergmann K; Lütjohann D Klin Padiatr; 2004; 216(2):67-9. PubMed ID: 15106076 [TBL] [Abstract][Full Text] [Related]
51. Long term follow-up of two sibs with an autosomal recessive form of chrondrodysplasia punctata and epilepsy. Stoll C; Pauly F; Steib JP Genet Couns; 2004; 15(4):411-20. PubMed ID: 15658616 [TBL] [Abstract][Full Text] [Related]
53. Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type. Menten B; Buysse K; Vandesompele J; De Smet E; De Paepe A; Speleman F; Mortier G Eur J Med Genet; 2005; 48(3):301-9. PubMed ID: 16179225 [TBL] [Abstract][Full Text] [Related]
55. Treatment of pes cavus in a patient with Charcot-Marie-Tooth disease. Colon MJ; Whitton KE; Schwartz N J Foot Surg; 1980; 19(1):41-4. PubMed ID: 7240666 [No Abstract] [Full Text] [Related]