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Journal Abstract Search
103 related items for PubMed ID: 3377015
1. Oculoauriculovertebral dysplasia. Ardingen HH, Lin AE. Am J Med Genet; 1988 Mar; 29(3):691-4. PubMed ID: 3377015 [No Abstract] [Full Text] [Related]
2. Goldenhar syndrome (oculo-auriculo-vertebral dysplasia) in new born. Mishra PC, Mathur GP, Mathur S, Singh YD. Indian Pediatr; 1981 Dec; 18(12):927-8. PubMed ID: 7343493 [No Abstract] [Full Text] [Related]
3. Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia. Regenbogen L, Godel V, Goya V, Goodman RM. Clin Genet; 1982 Mar; 21(3):161-7. PubMed ID: 7094392 [No Abstract] [Full Text] [Related]
4. Hemifacial microsomia and variants: pedigree data. Rollnick BR, Kaye CI. Am J Med Genet; 1983 Jun; 15(2):233-53. PubMed ID: 6881197 [Abstract] [Full Text] [Related]
5. Oculoauriculovertebral anomaly: variability and causal heterogeneity. Rollnick BR. Am J Med Genet Suppl; 1988 Jun; 4():41-53. PubMed ID: 3144985 [Abstract] [Full Text] [Related]
6. Malformations of the auricle: isolated and in syndromes. IV. Cumulative pedigree data. Kaye CI, Rollnick BR, Pruzansky S. Birth Defects Orig Artic Ser; 1979 Jun; 15(5C):163-9. PubMed ID: 526600 [No Abstract] [Full Text] [Related]
8. Goldenhar syndrome (oculo-auriculo-vertebral dysplasia) in a twin new born baby. Faridi MM, Ahmad S, Moonis R, Ansari Z, Bhargava SK. Indian J Pediatr; 1986 Jun; 53(2):291-4. PubMed ID: 3744465 [No Abstract] [Full Text] [Related]
9. Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q). Herman GE, Greenberg F, Ledbetter DH. Am J Med Genet; 1988 Apr; 29(4):909-15. PubMed ID: 3400736 [Abstract] [Full Text] [Related]
10. Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome. Wilson GN, Barr M. J Craniofac Genet Dev Biol; 1983 Apr; 3(4):313-6. PubMed ID: 6662905 [Abstract] [Full Text] [Related]
11. Discordance of signs in monozygotic twins concordant for the Goldenhar anomaly. Ryan CA, Finer NN, Ives E. Am J Med Genet; 1988 Apr; 29(4):755-61. PubMed ID: 3400721 [Abstract] [Full Text] [Related]
12. IVF and Goldenhar syndrome. Yovich J, Mulcahy M, Matson P. J Med Genet; 1987 Oct; 24(10):644. PubMed ID: 3681913 [No Abstract] [Full Text] [Related]
15. [Goldenhar syndrome. Discordance in monozygotic twins]. Gómez García A, Vargas Torcal F, Payá Abad EA. An Esp Pediatr; 1984 Mar 15; 20(4):400-2. PubMed ID: 6732066 [Abstract] [Full Text] [Related]
16. Paroxysmal intracranial hypertension and oculoauriculovertebral dysplasia. Hennekam RC, Van Nieuwenhuizen O, Gooskens RH. J Genet Hum; 1989 Dec 15; 37(4-5):437-8. PubMed ID: 2635720 [No Abstract] [Full Text] [Related]
17. TCOF1 mutations excluded from a role in other first and second branchial arch-related disorders. Splendore A, Passos-Bueno MR, Jabs EW, Van Maldergem L, Wulfsberg EA. Am J Med Genet; 2002 Aug 15; 111(3):324-7. PubMed ID: 12210332 [No Abstract] [Full Text] [Related]
18. [A case of oculoauriculovertebral dysplasia associated with cleft lip (author's transl)]. Ko K, Nakamura K, Uchiyama T, Turuki T, Inoue T, Ogata S, Matuo T, Mori Y. Shikwa Gakuho; 1979 Nov 15; 79(11):2171-6. PubMed ID: 298043 [No Abstract] [Full Text] [Related]
19. Progressive hearing loss in Goldenhar's syndrome. Parving A. Scand Audiol; 1978 Nov 15; 7(2):101-3. PubMed ID: 756070 [Abstract] [Full Text] [Related]