Related Articles by Review for PMID: 18855923

Year	Number of Results
1988	2
1991	1
1992	1
1993	1
1998	1
2004	1
2006	1
2007	1
2008	1
2009	1
2015	1
2016	1
2024	0

1

Familial oculoauriculovertebral sequence with lymphoma in one sibling.

Amalnath SD, Subrahmanyam DK, Dutta TK, Shenoy P. Amalnath SD, et al. Am J Med Genet A. 2008 Dec 1;146A(23):3082-5. doi: 10.1002/ajmg.a.32258. Am J Med Genet A. 2008. PMID: 18855923 No abstract available.

2

Oculoauriculovertebral spectrum: report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature.

Vendramini-Pittoli S, Kokitsu-Nakata NM. Vendramini-Pittoli S, et al. Clin Dysmorphol. 2009 Apr;18(2):67-77. doi: 10.1097/MCD.0b013e328323a7dd. Clin Dysmorphol. 2009. PMID: 19305190 Review.

3

An interesting case presentation: pulmonary malformations associated with oculoauriculovertebral dysplasia (Goldenhar anomalad).

Downing GJ, Kilbride H. Downing GJ, et al. J Perinatol. 1991 Jun;11(2):190-2. J Perinatol. 1991. PMID: 1890482 Review.

4

Anomalous inferior and superior venae cavae with oculoauriculovertebral defect: review of Goldenhar complex and malformations of left-right asymmetry.

Lin HJ, Owens TR, Sinow RM, Fu PC Jr, DeVito A, Beall MH, Lachman RS. Lin HJ, et al. Am J Med Genet. 1998 Jan 6;75(1):88-94. doi: 10.1002/(sici)1096-8628(19980106)75:1<88::aid-ajmg18>3.0.co;2-o. Am J Med Genet. 1998. PMID: 9450864 Review.

5

Orthopaedic manifestations of Goldenhar syndrome.

Avon SW, Shively JL. Avon SW, et al. J Pediatr Orthop. 1988 Nov-Dec;8(6):683-6. doi: 10.1097/01241398-198811000-00010. J Pediatr Orthop. 1988. PMID: 3056973 Review.

6

Oculoauriculovertebral spectrum and cerebral anomalies.

Schrander-Stumpel CT, de Die-Smulders CE, Hennekam RC, Fryns JP, Bouckaert PX, Brouwer OF, da Costa JJ, Lommen EJ, Maaswinkel-Mooy PD. Schrander-Stumpel CT, et al. J Med Genet. 1992 May;29(5):326-31. doi: 10.1136/jmg.29.5.326. J Med Genet. 1992. PMID: 1583660 Free PMC article. Review.

7

Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.

Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL. Kobrynski L, et al. Am J Med Genet. 1993 Apr 1;46(1):68-71. doi: 10.1002/ajmg.1320460111. Am J Med Genet. 1993. PMID: 8494034 Review.

8

7q21.11 Microdeletion in a Neonate With Goldenhar Syndrome: Case Report and a Literature Review.

Puvabanditsin S, February M, Francois L, Garrow E, Bruno C, Mehta R. Puvabanditsin S, et al. Cleft Palate Craniofac J. 2016 Mar;53(2):249-52. doi: 10.1597/14-308. Epub 2015 Jun 11. Cleft Palate Craniofac J. 2016. PMID: 26068384 Review.

9

Oculoauriculovertebral anomaly: variability and causal heterogeneity.

Rollnick BR. Rollnick BR. Am J Med Genet Suppl. 1988;4:41-53. doi: 10.1002/ajmg.1320310510. Am J Med Genet Suppl. 1988. PMID: 3144985 Review.

10

Novel deformity of the mandible in oculo-auriculo-vertebral spectrum: case report and literature review.

Caccamese JF Jr, Costello BJ, Mooney MP. Caccamese JF Jr, et al. J Oral Maxillofac Surg. 2006 Aug;64(8):1278-82. doi: 10.1016/j.joms.2006.03.034. J Oral Maxillofac Surg. 2006. PMID: 16860224 Review. No abstract available.

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