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.
87 related articles for article (PubMed ID: 6426025)
1. [Conradi chondrodysplasia--stippled disease of the epiphyses]. Lupaşcu E; Negrescu D; Mihai A; Burdea M Rev Pediatr Obstet Ginecol Pediatr; 1984; 33(1):85-9. PubMed ID: 6426025 [No Abstract] [Full Text] [Related]
2. [Localized stippled epiphyses and dysmorphia of the nose (minor form of Conradi Hünermann disease). (author's transl)]. BETOULIERES P; Ferran JL; Bassini P; Del Socorro P; Bonnet H; Jean R J Radiol Electrol Med Nucl; 1974 Dec; 55(12):877-81. PubMed ID: 4455873 [No Abstract] [Full Text] [Related]
7. [The congenital disease of stippled epiphyses. (Apropos of 2 cases)]. Christiaens L; Dubois O; Nuyts JP Lille Med; 1965; 10(6):591-8. PubMed ID: 5834762 [No Abstract] [Full Text] [Related]
8. [Alcohol embryopathy with symptomatic chondrodysplasia punctata. The 4th published case]. Paditz E; Rupprecht E Helv Paediatr Acta; 1985 Apr; 40(1):61-8. PubMed ID: 3855176 [TBL] [Abstract][Full Text] [Related]
9. Conradi-Hunerman syndrome. Case report. Hochman M; Fee WE Ann Otol Rhinol Laryngol; 1987; 96(5):565-8. PubMed ID: 3674654 [TBL] [Abstract][Full Text] [Related]
10. [Chondrodysplasia punctata (the Conradi-Hünermann syndrome). A clinical case report and review of the literature]. Omobono E; Goetsch W Minerva Pediatr; 1993 Mar; 45(3):117-21. PubMed ID: 8341225 [TBL] [Abstract][Full Text] [Related]
11. [Congenital disease of stippled epiphyses]. Sacrez R; Lévy JM; Gigonnet JM; Walter JP; Roth A Arch Fr Pediatr; 1965 Oct; 22(8):991-1000. PubMed ID: 5855786 [No Abstract] [Full Text] [Related]
12. 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]
13. A rare lethal case of chondrodysplasia punctata with extensive airway involvement. Dewan P; Rai A; Gupta N; Shah D; Faridi MM Fetal Pediatr Pathol; 2012 Jun; 31(3):134-9. PubMed ID: 22413868 [TBL] [Abstract][Full Text] [Related]
14. Chondrodysplasia punctata: case report and review of audiological and ENT features. Murdin L; Sirimanna T; Hartley BE; Holder SE J Laryngol Otol; 2006 Mar; 120(3):233-6. PubMed ID: 16359148 [TBL] [Abstract][Full Text] [Related]
15. [Association of stippled epiphyses and trisomy 21 in a newborn infant]. Sénécal J; Boguais MT; Le Berre C; Le Marec B Arch Fr Pediatr; 1968 Oct; 25(8):958-9. PubMed ID: 4235169 [No Abstract] [Full Text] [Related]
19. Peroxisomal enzyme deficiency in the Conradi-Hunerman form of chondrodysplasia punctata. Holmes RD; Wilson GN; Hajra AK N Engl J Med; 1987 Jun; 316(25):1608. PubMed ID: 3587298 [No Abstract] [Full Text] [Related]
20. [CONTRIBUTION TO THE CLINICAL PICTURE OF CHONDRODYSTROPHIA CALCIFICANS CONGENITA (CONRADI-HUENERMANN)]. MAYER H; WOLLENSAK J; DAMEROW R Z Kinderheilkd; 1964 Nov; 91():282-96. PubMed ID: 14333491 [No Abstract] [Full Text] [Related] [Next] [New Search]