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.
142 related articles for article (PubMed ID: 139022)
81. [On a case of chondrodystrophia calcificans contenita]. Arcangeli A; Benevolo A; Ascarelli A; Bortolotti G Arch Ital Pediatr Pueric; 1966; 24(5):418-28. PubMed ID: 6011420 [No Abstract] [Full Text] [Related]
82. Severe pulmonary arterial stenoses in Conradi-Hünermann disease. Trowitzsch E; Richter R; Eisenberg W; Kallfelz HC Eur J Pediatr; 1986 Apr; 145(1-2):116-8. PubMed ID: 3732312 [TBL] [Abstract][Full Text] [Related]
83. X-linked dominant ichthyosis with peroxisomal deficiency. An ultrastructural and ultracytochemical study of the Conradi-Hünermann syndrome and its murine homologue, the bare patches mouse. Emami S; Hanley KP; Esterly NB; Daniallinia N; Williams ML Arch Dermatol; 1994 Mar; 130(3):325-36. PubMed ID: 8129411 [TBL] [Abstract][Full Text] [Related]
84. [Conradi-Hünermann-Happle syndrome with unilateral distribution]. Hello M; David A; Barbarot S Ann Dermatol Venereol; 2010 Jan; 137(1):44-7. PubMed ID: 20110068 [TBL] [Abstract][Full Text] [Related]
85. Conradi-Hünermann syndrome with unilateral distribution. Corbí MR; Conejo-Mir JS; Linares M; Jiménez G; Rodríguez Cañas T; Navarrete M Pediatr Dermatol; 1998; 15(4):299-303. PubMed ID: 9720698 [TBL] [Abstract][Full Text] [Related]
86. Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype. Offiah AC; Mansour S; Jeffrey I; Nash R; Whittock N; Pyper R; Bewley S; Clayton PT; Hall CM J Med Genet; 2003 Dec; 40(12):e129. PubMed ID: 14684697 [No Abstract] [Full Text] [Related]
87. Ultrastructural observations on stumpy (stm), a new chondrodystrophic mutant in the mouse. Johnson DR J Embryol Exp Morphol; 1977 Jun; 39():279-84. PubMed ID: 886261 [TBL] [Abstract][Full Text] [Related]
88. [Chondrodysplasia punctata congenita: a genetic heterogenous disease]. Hack WW; Derksen-Samson JF; Grimberg RT; van der Harten JJ Tijdschr Kindergeneeskd; 1984 Feb; 52(1):16-23. PubMed ID: 6710469 [TBL] [Abstract][Full Text] [Related]
89. Chondrodysplasia punctata. Report of two cases. Andersen PE; Justesen P Skeletal Radiol; 1987; 16(3):223-6. PubMed ID: 3589739 [TBL] [Abstract][Full Text] [Related]
96. [Autosomal dominant chondrodysplasia punctata with laryngo-tracheal calcification. Presentation of 2 cases]. Camera G; Pedrotti D; Follesa MG; Centa A Pathologica; 1985; 77(1052):693-8. PubMed ID: 3842991 [No Abstract] [Full Text] [Related]
97. Radiological case of the month. Chondrodysplasia punctata: Conradi-Hünermann form. Young LW; King TD; Dunn D; Faygenbaum D Am J Dis Child; 1979 Nov; 133(11):1191-3. PubMed ID: 507012 [No Abstract] [Full Text] [Related]
98. [Conradi-Hünermann syndrome in a newborn infant]. Maszkiewicz W; Kagan-Sypula I; Ginczewska T Pediatr Pol; 1978 Jul; 53(7):889-92. PubMed ID: 693139 [No Abstract] [Full Text] [Related]
99. [Chondrodysplasia punctata. 3 new cases and review of the Spanish literature]. Aguilera Olmos R; Tripiana López JL; Vitoria Miñana I; Nacher Fernández A; Buesa E An Esp Pediatr; 1986 Aug; 25(2):105-10. PubMed ID: 3752745 [TBL] [Abstract][Full Text] [Related]
100. The role of the abnormalities in the distal pathway of cholesterol biosynthesis in the Conradi-Hünermann-Happle syndrome. Cañueto J; Girós M; González-Sarmiento R Biochim Biophys Acta; 2014 Mar; 1841(3):336-44. PubMed ID: 24036494 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]