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7. Chondrodysplasia Punctata: A Case Report of Fetal Warfarin Syndrome. Songmen S; Panta OB; Paudel SS; Ghimire RK J Nepal Health Res Counc; 2017 Jan; 15(1):81-84. PubMed ID: 28714498 [TBL] [Abstract][Full Text] [Related]
8. Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism. Menger H; Lin AE; Toriello HV; Bernert G; Spranger JW Am J Med Genet; 1997 Oct; 72(2):129-34. PubMed ID: 9382132 [TBL] [Abstract][Full Text] [Related]
9. [Analysis of clinical manifestation and genetic mutation in a child with X-linked chondrodysplasia punctata 2]. Chang G; Zhou Y; Yin L; Gu L; Ying D; Chen H; Wang X; Wang J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):527-530. PubMed ID: 30098249 [TBL] [Abstract][Full Text] [Related]
11. Pregnancy outcome of first trimester exposure to the vitamin K antagonist phenprocoumon depends on duration of treatment. Hüttel E; Padberg S; Meister R; Beck E; Schaefer C Thromb Haemost; 2017 May; 117(5):870-879. PubMed ID: 28229160 [TBL] [Abstract][Full Text] [Related]
18. Prenatal exposure to phenytoin, facial development, and a possible role for vitamin K. Howe AM; Lipson AH; Sheffield LJ; Haan EA; Halliday JL; Jenson F; David DJ; Webster WS Am J Med Genet; 1995 Sep; 58(3):238-44. PubMed ID: 8533825 [TBL] [Abstract][Full Text] [Related]
19. Dominant sex-linked inherited chondrodysplasia punctata: a distinct type of chondrodysplasia punctata. Manzke H; Christophers E; Wiedemann HR Clin Genet; 1980 Feb; 17(2):97-107. PubMed ID: 7363504 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of nonrhizomelic chondrodysplasia punctata (Conradi-Hünermann syndrome). Pryde PG; Bawle E; Brandt F; Romero R; Treadwell MC; Evans MI Am J Med Genet; 1993 Sep; 47(3):426-31. PubMed ID: 8135294 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]