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3. [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]
4. Vitreoretinal abnormalities in the Conradi-Hunermann form of chondrodysplasia punctata. Ramkissoon YD; Mayer EJ; Gibbon C; Haynes RJ Br J Ophthalmol; 2004 Jul; 88(7):973-4. PubMed ID: 15205255 [No Abstract] [Full Text] [Related]
5. Lethal chondrodysplasia punctata, Conradi Hünermann subtype A, one case. Gaulier A; Chastagner C; Leloc'h H; Babin C Pathol Res Pract; 1987 Feb; 182(1):72-9. PubMed ID: 3588407 [TBL] [Abstract][Full Text] [Related]
6. Diffuse erythema and dry scales in a female infant. X-linked dominant Conradi-Hunermann-Happle (CHH) syndrome. Ali L; Ricotti C; Li L; Calame A; Brouha B; Helm T; Cockerell C Am J Dermatopathol; 2011 May; 33(3):316, 331. PubMed ID: 20802302 [No Abstract] [Full Text] [Related]
11. [Deficit of cellular chemotaxis in a case of chondrodystrophic punctata of the Conradi-Hunermann type]. Galluzzi F; De Martino M; Salti R; Varone D; La Cauza C Minerva Pediatr; 1980 Apr; 32(8):555-62. PubMed ID: 7393188 [No Abstract] [Full Text] [Related]
12. Conradi-Hünermann-Happle syndrome associated with severe hypocalcemia in a newborn. Dykman M; Voller LM; Boull C Pediatr Dermatol; 2022 Jul; 39(4):657-658. PubMed ID: 35355312 [TBL] [Abstract][Full Text] [Related]
13. Normal peroxisomal function and absent skeletal manifestations in Conradi-Hünermann syndrome. Prendiville JS; Zaparackas ZG; Esterly NB Arch Dermatol; 1991 Apr; 127(4):539-42. PubMed ID: 2006879 [TBL] [Abstract][Full Text] [Related]