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Results: 13

1.

Clinical and genetic characteristics for the Urofacial Syndrome (UFS).

Tu Y, Yang P, Yang J, Xu Y, Xiong F, Yu Q, Gu W, Pond D, Mendelsohn N, Lachmeijer GA, Zhang S, Wang CY.

Int J Clin Exp Pathol. 2014 Apr 15;7(5):1842-8. eCollection 2014. Review.

PMID:
24966895
[PubMed - in process]
Free PMC Article
2.

In vivo confocal microscopy in goldenhar syndrome: a case report.

Triolo G, Ferrari G, Doglioni C, Rama P.

BMC Ophthalmol. 2013 Oct 16;13:55. doi: 10.1186/1471-2415-13-55.

PMID:
24131730
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A Lebanese family with autosomal recessive oculo-auriculo-vertebral (OAV) spectrum and review of the literature: is OAV a genetically heterogeneous disorder?

Farra C, Yunis K, Yazbeck N, Majdalani M, Charafeddine L, Wakim R, Awwad J.

Appl Clin Genet. 2011 Jul 6;4:93-7. doi: 10.2147/TACG.S12643. Print 2011.

PMID:
23776370
[PubMed]
Free PMC Article
4.

45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationships.

Baynam G, Goldblatt J.

J Maxillofac Oral Surg. 2009 Sep;8(3):279-82. doi: 10.1007/s12663-009-0068-x. Epub 2009 Nov 21.

PMID:
23139526
[PubMed]
Free PMC Article
5.

Hemifacial microsomia with pulmonary hypoplasia.

Panigrahi I, Das RR, Marwaha RK.

BMJ Case Rep. 2010 May 16;2010. pii: bcr0420091759. doi: 10.1136/bcr.04.2009.1759.

PMID:
22750194
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Goldenhar syndrome: a cause of secondary immunodeficiency?

De Golovine S, Wu S, Hunter JV, Shearer WT.

Allergy Asthma Clin Immunol. 2012 Jul 2;8(1):10. doi: 10.1186/1710-1492-8-10.

PMID:
22747588
[PubMed]
Free PMC Article
7.

Solitary median maxillary central incisor in association with hemifacial microsomia: A rare case report and review of literature.

Utreja A, Zahid SN, Gupta R.

Contemp Clin Dent. 2011 Oct;2(4):385-9. doi: 10.4103/0976-237X.91810.

PMID:
22346174
[PubMed]
Free PMC Article
8.

Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up.

Rittler M, Cosentino V, López-Camelo JS, Murray JC, Wehby G, Castilla EE.

Am J Med Genet A. 2011 Jul;155A(7):1588-96. doi: 10.1002/ajmg.a.34046. Epub 2011 Jun 10.

PMID:
21671378
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Goldenhar syndrome: clinical features with orofacial emphasis.

Martelli H Jr, Miranda RT, Fernandes CM, Bonan PR, Paranaíba LM, Graner E, Coletta RD.

J Appl Oral Sci. 2010 Dec;18(6):646-9.

PMID:
21308299
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2.

Digilio MC, McDonald-McGinn DM, Heike C, Catania C, Dallapiccola B, Marino B, Zackai EH.

Am J Med Genet A. 2009 Dec;149A(12):2860-4. doi: 10.1002/ajmg.a.33034.

PMID:
19890921
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

'Inside-out', back-to-front: a model for clinical population genetic screening.

Shickle D, Harvey I.

J Med Genet. 1993 Jul;30(7):580-2.

PMID:
8411031
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Severe manifestations of oculoauriculovertebral spectrum in a cocaine exposed infant.

Lessick M, Vasa R, Israel J.

J Med Genet. 1991 Nov;28(11):803-4. No abstract available.

PMID:
1770540
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

J Med Genet. 1992 May;29(5):326-31. Review.

PMID:
1583660
[PubMed - indexed for MEDLINE]
Free PMC Article

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