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2. Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum. Johnson JP; Poskanzer LS; Sherman S Am J Med Genet; 1996 Jan; 61(2):134-9. PubMed ID: 8669439 [TBL] [Abstract][Full Text] [Related]
3. 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]
8. Frontonasal malformation and the oculoauriculovertebral spectrum: the oculoauriculofrontonasal syndrome. Casey HD; Braddock SR; Haskins RC; Carey JC; Morales L Cleft Palate Craniofac J; 1996 Nov; 33(6):519-23. PubMed ID: 8939380 [TBL] [Abstract][Full Text] [Related]
9. Failed intubation in a case of oculoauriculovertebral dysplasia (Goldenhar's syndrome). Mohandas K; Selvarajah S Med J Malaysia; 1988 Sep; 43(3):255-8. PubMed ID: 3241587 [No Abstract] [Full Text] [Related]
10. Temporal bone histopathologic findings in oculoauriculovertebral dysplasia. Goldenhar's syndrome. Sando I; Ikeda M Ann Otol Rhinol Laryngol; 1986; 95(4 Pt 1):396-400. PubMed ID: 3740715 [TBL] [Abstract][Full Text] [Related]
11. Goldenhar's syndrome: case report. Adeoye AO East Afr Med J; 2002 Sep; 79(9):502-4. PubMed ID: 12625694 [TBL] [Abstract][Full Text] [Related]
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13. Severe bilateral ocular features in Goldenhar's syndrome. Mc Alister JC; Olver JM; Hatter T J Pediatr Ophthalmol Strabismus; 2001; 38(1):44-6. PubMed ID: 11201919 [No Abstract] [Full Text] [Related]
14. Characterization of facial paresis in hemifacial microsomia. Cline JM; Hicks KE; Patel KG Otolaryngol Head Neck Surg; 2014 Feb; 150(2):188-93. PubMed ID: 24492209 [TBL] [Abstract][Full Text] [Related]
15. Preterm diagnosis of choristoma and choroidal coloboma in Goldenhar's syndrome. Herwig MC; Gembruch U; Born M; Gevensleben H; Loeffler KU; Müller AM Pediatr Dev Pathol; 2011; 14(4):322-6. PubMed ID: 21345085 [TBL] [Abstract][Full Text] [Related]
17. Hemifacial microsomia in a newborn with hypoplastic skin lesions, an eyelid skin tag, and microphthalmia: an unusual presentation of Delleman syndrome. Ming JE; Katowitz J; McDonald-McGinn DM; Schnur RE; Hunter JV; Zackai EH Clin Dysmorphol; 1998 Oct; 7(4):279-83. PubMed ID: 9823495 [TBL] [Abstract][Full Text] [Related]
18. Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC). Bergmann C; Zerres K; Peschgens T; Senderek J; Hörnchen H; Rudnik-Schöneborn S Am J Med Genet A; 2003 Aug; 121A(2):151-5. PubMed ID: 12910495 [TBL] [Abstract][Full Text] [Related]
19. Goldenhar's syndrome associated with occipital meningoencephalocele--case report. Kita D; Munemoto S; Ueno Y; Fukuda A Neurol Med Chir (Tokyo); 2002 Aug; 42(8):354-5. PubMed ID: 12206491 [TBL] [Abstract][Full Text] [Related]
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