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3. [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]
8. Conradi-Hünermann disease. Case report and mini-review. Paltzik RL; Ente G; Penzer PH; Goldblum LM Cutis; 1982 Feb; 29(2):174-180. PubMed ID: 7060406 [No Abstract] [Full Text] [Related]
9. 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]
10. Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome. Case study and review of peroxisomal disorders in relation to skin disease. Emami S; Rizzo WB; Hanley KP; Taylor JM; Goldyne ME; Williams ML Arch Dermatol; 1992 Sep; 128(9):1213-22. PubMed ID: 1519936 [TBL] [Abstract][Full Text] [Related]
11. The nature of cartilage stippling in chondrodysplasia punctata: histopathological study of Conradi-Hünermann syndrome. Pazzaglia UE; Zarattini G; Donzelli C; Benetti A; Bondioni MP; Groli C Fetal Pediatr Pathol; 2008; 27(2):71-81. PubMed ID: 18568995 [TBL] [Abstract][Full Text] [Related]
12. Conradi-Hünermann syndrome with ocular anomalies. Tanaka Y; Saitoh A; Taniguchi H; Oba K; Kitaoka T; Amemiya T Ophthalmic Genet; 1999 Dec; 20(4):271-4. PubMed ID: 10617926 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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]
15. [Conradi syndrome and inflammatory lineal verrucose epidermal nevus]. Román Maciá P; Albero Blanes F; de Teresa Parreño L Actas Dermosifiliogr; 1980; 71(5-6):209-14. PubMed ID: 7468331 [No Abstract] [Full Text] [Related]
16. 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]
17. 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]
19. Evidence of postzygotic mosaicism in a transmitted form of Conradi-Hunermann-Happle syndrome associated with a novel EBP mutation. Morice-Picard F; Kostrzewa E; Wolf C; Benlian P; Taïeb A; Lacombe D Arch Dermatol; 2011 Sep; 147(9):1073-6. PubMed ID: 21931045 [TBL] [Abstract][Full Text] [Related]