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2. Goldenhar syndrome and hemifacial microsomia: observations on three patients. Thomas P Eur J Pediatr; 1980 May; 133(3):287-92. PubMed ID: 7389743 [TBL] [Abstract][Full Text] [Related]
5. [Report of an atypical case of Goldenhar syndrome]. Fiore C; Santoni G; Lungarotti S; Signorini E Ophthalmologica; 1983; 186(3):162-8. PubMed ID: 6843966 [TBL] [Abstract][Full Text] [Related]
6. Associated malformations of the eye and the ear. The Goldenhar syndrome. Orzalesi N; Lostia S; Loi M; Tulli P Ophthalmologica; 1978; 177(5):237-44. PubMed ID: 740353 [No Abstract] [Full Text] [Related]
7. [Lipoma of the corpus callosum as a constituent of Goldenhar syndrome]. Thommen L; Bubl R; Fliegel CP Monatsschr Kinderheilkd; 1986 Aug; 134(8):541-3. PubMed ID: 3773922 [TBL] [Abstract][Full Text] [Related]
17. A patient with median cleft face anomaly and bilateral Goldenhar anomaly. Musarella MA; Young ID Am J Med Genet Suppl; 1986; 2():135-41. PubMed ID: 3146283 [TBL] [Abstract][Full Text] [Related]
18. Hemifacial microsomia and hypodontia: a case report. Alkumru HN; Cölok G J Oral Rehabil; 1992 Nov; 19(6):671-5. PubMed ID: 1469503 [TBL] [Abstract][Full Text] [Related]
19. [Goldenhar syndrome with neuroparalytic keratitis and lacrimal hyposecretion]. Reny A; George JL; Brichet M; Hachet E; Gdal'on M Bull Soc Ophtalmol Fr; 1982; 82(8-9):1159-62. PubMed ID: 6984665 [No Abstract] [Full Text] [Related]