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Items: 1 to 20 of 102

1.

Familial oculoauriculovertebral sequence with lymphoma in one sibling.

Amalnath SD, Subrahmanyam DK, Dutta TK, Shenoy P.

Am J Med Genet A. 2008 Dec 1;146A(23):3082-5. doi: 10.1002/ajmg.a.32258. No abstract available.

PMID:
18855923
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.

Clin Dysmorphol. 2009 Apr;18(2):67-77. doi: 10.1097/MCD.0b013e328323a7dd. Review.

PMID:
19305190
3.

31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings.

Engiz O, Balci S, Unsal M, Ozer S, Oguz KK, Aktas D.

Genet Couns. 2007;18(3):277-88.

PMID:
18019368
4.

Goldenhar complex: a further case with uncommon associated anomalies.

Zelante L, Gasparini P, Castriota Scanderbeg A, Dimitri L, Criconia M, Gorlin RJ.

Am J Med Genet. 1997 Apr 14;69(4):418-21.

PMID:
9098494
5.

Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1.

Goodin K, Prucka S, Woolley AL, Kohlhase J, Smith RJ, Grant J, Robin NH.

Am J Med Genet A. 2009 Mar;149A(3):535-8. doi: 10.1002/ajmg.a.32673. No abstract available.

PMID:
19213029
6.

Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.

Ng YY, Hu JM, Su PH, Chen JY, Yang MS, Chen SJ.

Acta Paediatr Taiwan. 2006 May-Jun;47(3):142-5.

PMID:
17078468
7.

[Oculoauriculovertebral syndrome (Goldenhar syndrome) associated with Hirschsprung disease].

Lankosz-Lauterbach J, Sanak M.

Pediatr Pol. 1987 Apr;62(4):249-52. Polish. No abstract available.

PMID:
3670916
8.

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. No abstract available.

PMID:
7094392
9.

[Goldenhar syndrome and arachnoid cyst].

Hajje MJ, Nachanakian A, Haddad J.

Arch Pediatr. 2003 Apr;10(4):353-4. French. No abstract available.

PMID:
12818762
10.

Congenital ameloblastic fibroma in association with oculoauriculovertebral spectrum.

Naidoo LC, Stephen LX.

Int J Pediatr Otorhinolaryngol. 1998 May 15;43(3):283-8.

PMID:
9663951
11.

Oculoauriculovertebral complex with an atypical cause of obstructive sleep apnea.

Kourelis K, Gouma P, Naxakis S, Kalogeropoulou C, Goumas P.

Int J Pediatr Otorhinolaryngol. 2009 Mar;73(3):481-5. doi: 10.1016/j.ijporl.2008.11.004. Epub 2008 Dec 27.

PMID:
19111916
12.

[Goldenhar syndrome associated to posterior urethral valves].

Palacios A, Pedro Carvalho A, de Castro R, Reis A.

Arch Esp Urol. 2007 Jan-Feb;60(1):69-71. Spanish.

PMID:
17408176
13.

[Goldenhar syndrome (oculoauriculovertebral dysplasia)].

Danes J, Bartosová L.

Cesk Radiol. 1986 Nov;40(6):388-93. Czech. No abstract available.

PMID:
3802294
14.

Autosomal dominant Goldenhar syndrome.

Godel V, Regenbogen L, Goya V, Goodman RM.

Birth Defects Orig Artic Ser. 1982;18(6):621-8. No abstract available.

PMID:
7171780
15.

Goldenhar syndrome with multiple additional anomalies.

Jaison SG, Batra N.

Indian J Ophthalmol. 1996 Mar;44(1):42-4. No abstract available.

16.

Rare associations with Goldenhar syndrome.

Vatwani V, Verma N, Palta SC, Dogra BB.

Indian Pediatr. 1994 Jan;31(1):72-3. No abstract available.

PMID:
7883328
17.

Oculoauriculovertebral anomaly: variability and causal heterogeneity.

Rollnick BR.

Am J Med Genet Suppl. 1988;4:41-53. Review.

PMID:
3144985
18.

Oculoauriculovertebral dysplasia.

Ardingen HH, Lin AE.

Am J Med Genet. 1988 Mar;29(3):691-4. No abstract available.

PMID:
3377015
19.

The syndrome of goldenhar affecting two siblings.

Krause U.

Acta Ophthalmol (Copenh). 1970;48(3):494-9. No abstract available.

PMID:
5536008
20.

A novel association in a family with oculo-auriculo-vertebral spectrum and x-linked ichthyosis.

Rivera-Vega MR, Dueñas E, Jimenez-Vaca AL, Valdes-Flores M, Gonzalez-Huerta LM, Kofman-Alfaro SH, Cuevas-Covarrubias SA.

Pediatr Dermatol. 2003 Mar-Apr;20(2):182-4. No abstract available.

PMID:
12657025
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