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6. Stippled epiphyses in the newborn and in infants. MOSEKILDE E Acta radiol; 1952; 37(3-4):291-307. PubMed ID: 14933209 [No Abstract] [Full Text] [Related]
9. Congenital stippled epiphyses. FORD GD; SCHNEIDER M; BRANDON JR Pediatrics; 1951 Sep; 8(3):380-92. PubMed ID: 14875454 [No Abstract] [Full Text] [Related]
10. [Stippled epiphyses (6 cases)]. Fall M; Niang I; Kuakuvi N; Martin L; Sanokho A; Senghor G; Sarr M; Sow D Dakar Med; 1979; 24(4):377-84. PubMed ID: 544218 [No Abstract] [Full Text] [Related]
11. [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]
12. [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]
13. [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]
16. [Cutaneous signs and symptoms of X-linked chondrodysplasia punctata in man and mouse]. Happle R Ann Dermatol Venereol; 1983; 110(10):803-6. PubMed ID: 6666923 [TBL] [Abstract][Full Text] [Related]
17. [Rhizomelic type of chondrodysplasia punctata in 2 sisters. Evidence for hereditary transmission of a recessive autosomic type]. Fabris C; Licata D; Martano C; Silengo M; Franceschini P Minerva Pediatr; 1981 Jan; 33(2):81-5. PubMed ID: 7242481 [No Abstract] [Full Text] [Related]
18. [Congenital disease of stippled epiphyses or fetal chondrodystrophic epiphysial calcinosis]. JEUNE M; LARBRE F; CARRON R; COUETTE I Arch Fr Pediatr; 1953; 10(9):914-42. PubMed ID: 13125647 [No Abstract] [Full Text] [Related]
19. [Contribution to the study of chondroangiopathia punctata congenita]. Rovei S; Centa A Pathologica; 1965; 57(853):259-66. PubMed ID: 5886560 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]