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Items: 1 to 20 of 133

1.

Transmission of the dysgnathia complex from mother to daughter.

Erlich MS, Cunningham ML, Hudgins L.

Am J Med Genet. 2000 Nov 27;95(3):269-74.

PMID:
11102934
2.

Otocephaly: report of five new cases and a literature review.

Faye-Petersen O, David E, Rangwala N, Seaman JP, Hua Z, Heller DS.

Fetal Pediatr Pathol. 2006 Sep-Oct;25(5):277-96.

PMID:
17438667
3.

Agnathia and associated malformations: a case report.

Brown DM, Marsh JL.

Cleft Palate J. 1990 Oct;27(4):415-8.

PMID:
2253390
4.

Airway management during an EXIT procedure for a fetus with dysgnathia complex.

Baker PA, Aftimos S, Anderson BJ.

Paediatr Anaesth. 2004 Sep;14(9):781-6.

PMID:
15330963
5.

Nonlethal case of otocephaly and its implications for treatment.

Shermak MA, Dufresne CR.

J Craniofac Surg. 1996 Sep;7(5):372-5.

PMID:
9133850
6.

[Apropos of a rare craniofacial abnormality of the 1st branchial arch].

Hsissen MA, Kadiri F, Detsouli M, Touhami M, Chekkoury IA, Benchakroun Y.

Rev Laryngol Otol Rhinol (Bord). 1996;117(2):141-4. French.

PMID:
8959936
7.

Aplasia of the first and second branchial arches.

Black FO, Myers EN, Rorke LB.

Arch Otolaryngol. 1973 Aug;98(2):124-8. No abstract available.

PMID:
4723764
8.

[Dysgnathia complex, a rare deviation].

Stuffken MJ, Tuinzing DB.

Ned Tijdschr Tandheelkd. 2008 Jul;115(7):394-6. Dutch.

PMID:
18686566
9.

Otocephalus: histopathology and three-dimensional reconstruction.

Hinojosa R, Green JD, Brecht K, Robb RA.

Otolaryngol Head Neck Surg. 1996 Jan;114(1):44-53.

PMID:
8570250
10.

Current perspectives on the etiology of agnathia-otocephaly.

Gekas J, Li B, Kamnasaran D.

Eur J Med Genet. 2010 Nov-Dec;53(6):358-66. doi: 10.1016/j.ejmg.2010.09.002. Epub 2010 Sep 16. Review.

PMID:
20849990
11.

Aplasia of the first and second branchial arches.

Leckie GB.

J Laryngol Otol. 1975 Dec;89(12):1263-9.

PMID:
1214103
12.

In utero diagnosis of agnathia, microstomia, and synotia.

Scholl HW Jr.

Obstet Gynecol. 1977 Jan;49(1 suppl):81-3.

PMID:
318738
13.

Severe Agnathia-Otocephaly Complex: Surgical Management and Longitudinal Follow-up From Birth Through Adulthood.

Golinko MS, Shetye P, Flores RL, Staffenberg DA.

J Craniofac Surg. 2015 Nov;26(8):2387-92. doi: 10.1097/SCS.0000000000002150.

PMID:
26517463
14.

Type II first branchial cleft anomaly.

Al-Mahdi AH, Al-Khurri LE, Atto GZ, Dhaher A.

J Craniofac Surg. 2013;24(5):1832-5. doi: 10.1097/SCS.0b013e3182997e12.

PMID:
24036791
15.

Complete mandibular agenesis. Report of a case.

Brecht K, Johnson CM 3rd.

Arch Otolaryngol. 1985 Feb;111(2):132-4.

PMID:
3977728
16.

[Particular form of hemifacial microsomia: clinical case].

Minervini G, Fiorentino G, Malzone A.

Arch Stomatol (Napoli). 1990 Apr-Jun;31(2):361-5. Italian. No abstract available.

PMID:
2097954
17.

Otocephaly or agnathia-synotia-microstomia syndrome: report of a case.

O'neill BM, Alessi AS, Petti NA.

J Oral Maxillofac Surg. 2003 Jul;61(7):834-7. No abstract available.

PMID:
12856261
19.

Computed tomographic reconstruction of a fetus with the dysgnathia complex (agnathia-otocephaly).

Rajan PV, Wing DA, Bocian M, McKeown A.

Prenat Diagn. 2007 Feb;27(2):130-2.

PMID:
17152114
20.

OTX2 mutations contribute to the otocephaly-dysgnathia complex.

Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W, Webb BD, Faye-Petersen O, Encha-Razavi F, Lequeux L, Vigouroux A, Yesilyurt A, Boyadjiev SA, Kayserili H, Loget P, Carles D, Sergi C, Puvabanditsin S, Chen CP, Etchevers HC, Katsanis N, Mercer CL, Calvas P, Jabs EW.

J Med Genet. 2012 Jun;49(6):373-9. doi: 10.1136/jmedgenet-2012-100892. Epub 2012 May 10.

PMID:
22577225

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