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Results: 1 to 20 of 94

1.

Auriculo-condylar syndrome. Confronting a diagnostic challenge.

Kokitsu-Nakata NM, Zechi-Ceide RM, Vendramini-Pittoli S, Romanelli Tavares VL, Passos-Bueno MR, Guion-Almeida ML.

Am J Med Genet A. 2012 Jan;158A(1):59-65. doi: 10.1002/ajmg.a.34337. Epub 2011 Nov 21.

PMID:
22105959
[PubMed - indexed for MEDLINE]
2.

Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity.

Masotti C, Oliveira KG, Poerner F, Splendore A, Souza J, Freitas Rda S, Zechi-Ceide R, Guion-Almeida ML, Passos-Bueno MR.

Eur J Hum Genet. 2008 Feb;16(2):145-52. Epub 2007 Nov 14.

PMID:
18000524
[PubMed - indexed for MEDLINE]
Free Article
3.

Auriculo-condylar syndrome is associated with highly variable ear and mandibular defects in multiple kindreds.

Storm AL, Johnson JM, Lammer E, Green GE, Cunniff C.

Am J Med Genet A. 2005 Oct 1;138A(2):141-5. Review.

PMID:
16114046
[PubMed - indexed for MEDLINE]
4.

Novel features in auriculo-condylar syndrome.

McGowan R, Murday V, Kinning E, Garcia S, Koppel D, Whiteford M.

Clin Dysmorphol. 2011 Jan;20(1):1-10. doi: 10.1097/MCD.0b013e32833e56f5.

PMID:
20733479
[PubMed - indexed for MEDLINE]
5.

Auriculo-condylar syndrome.

Papagrigorakis MJ, Karamolegou M, Vilos G, Apostolidis C, Karamesinis K, Synodinos PN.

Angle Orthod. 2012 May;82(3):556-64. doi: 10.2319/052911-356.1. Epub 2011 Nov 3.

PMID:
22050072
[PubMed - indexed for MEDLINE]
6.

Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?

Priolo M, Lerone M, Rosaia L, Calcagno EP, Sadeghi AK, Ghezzi F, Ravazzolo R, Silengo M.

Clin Dysmorphol. 2000 Oct;9(4):277-80. Review.

PMID:
11045585
[PubMed - indexed for MEDLINE]
7.

New syndrome? Prominent, constricted ears with malformed condyle of the mandible.

Jampol M, Repetto G, Keith DA, Curtin H, Remensynder J, Holmes LB.

Am J Med Genet. 1998 Feb 17;75(5):449-52.

PMID:
9489786
[PubMed - indexed for MEDLINE]
8.

Auriculo-condylar syndrome: further evidence for a new disorder.

Guion-Almeida ML, Kokitsu-Nakata NM, Zechi-Ceide RM, Vendramini S.

Am J Med Genet. 1999 Sep 10;86(2):130-3.

PMID:
10449647
[PubMed - indexed for MEDLINE]
9.

Clinical and radiographic features of the lacrimo-auriculo-dento-digital syndrome.

Murdoch-Kinch CA, Miles DA.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1996 Jun;81(6):727-35.

PMID:
8784906
[PubMed - indexed for MEDLINE]
10.

Auriculo-condylar syndrome: additional patients.

Guion-Almeida ML, Zechi-Ceide RM, Vendramini S, Kokitsu-Nakata NM.

Am J Med Genet. 2002 Oct 1;112(2):209-14.

PMID:
12244558
[PubMed - indexed for MEDLINE]
11.

Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutations.

Kido Y, Gordon CT, Sakazume S, Ben Bdira E, Dattani M, Wilson LC, Lyonnet S, Murakami N, Cunningham ML, Amiel J, Nagai T.

Am J Med Genet A. 2013 Sep;161A(9):2339-46. doi: 10.1002/ajmg.a.36066. Epub 2013 Aug 2.

PMID:
23913798
[PubMed - indexed for MEDLINE]
12.

A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.

Rieder MJ, Green GE, Park SS, Stamper BD, Gordon CT, Johnson JM, Cunniff CM, Smith JD, Emery SB, Lyonnet S, Amiel J, Holder M, Heggie AA, Bamshad MJ, Nickerson DA, Cox TC, Hing AV, Horst JA, Cunningham ML.

Am J Hum Genet. 2012 May 4;90(5):907-14. doi: 10.1016/j.ajhg.2012.04.002. Erratum in: Am J Hum Genet. 2012 Aug 10;91(2):397. Am J Hum Genet. 2012 Jun 8;90(6):1116.

PMID:
22560091
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Ossicular fusion and cholesteatoma in auriculo-condylar syndrome: in vivo evidence of arrest of embryogenesis.

Propst EJ, Ngan BY, Mount RJ, Martin-Munoz D, Blaser S, Harrison RV, Cushing SL, Papsin BC.

Laryngoscope. 2013 Feb;123(2):528-32. doi: 10.1002/lary.23492. Epub 2012 Aug 2.

PMID:
22865651
[PubMed - indexed for MEDLINE]
14.

The correction of auricular and mandibular deformities in auriculo-condylar syndrome.

Ozturk S, Sengezer M, Isik S, Gul D, Zor F.

J Craniofac Surg. 2005 May;16(3):489-92. Erratum in: J Craniofac Surg. 2005 Jul;16(4):743. Zor, Fatih [added].

PMID:
15915123
[PubMed - indexed for MEDLINE]
15.

Autosomal dominant isolated question mark ear.

Shkalim V, Eliaz N, Linder N, Merlob P, Basel-Vanagaite L.

Am J Med Genet A. 2008 Sep 1;146A(17):2280-3. doi: 10.1002/ajmg.a.32452.

PMID:
18680186
[PubMed - indexed for MEDLINE]
16.

Hemifacial microsomia and hypodontia: a case report.

Alkumru HN, Cölok G.

J Oral Rehabil. 1992 Nov;19(6):671-5.

PMID:
1469503
[PubMed - indexed for MEDLINE]
17.

Question mark ears and post-auricular tags.

Gerkes EH, van Ravenswaaij CM, van Essen AJ.

Eur J Med Genet. 2008 May-Jun;51(3):264-7. doi: 10.1016/j.ejmg.2008.01.002. Epub 2008 Jan 30.

PMID:
18314001
[PubMed - indexed for MEDLINE]
18.

[Agnathia, microstomia, synotia].

Monaco R, Ferbo U, Pugliese A, De Lieto G, Nazzaro G.

Pathologica. 1989 May-Jun;81(1073):291-3. Review. Italian.

PMID:
2701584
[PubMed - indexed for MEDLINE]
19.

Rippling muscle disease: evidence for phenotypic and genetic heterogeneity.

So YT, Zu L, Barraza C, Figueroa KP, Pulst SM.

Muscle Nerve. 2001 Mar;24(3):340-4.

PMID:
11353417
[PubMed - indexed for MEDLINE]
20.

A range of condylar hypoplasia exists in Treacher Collins syndrome.

Travieso R, Chang CC, Terner JS, Beckett J, Wong K, Teng E, Steinbacher DM.

J Oral Maxillofac Surg. 2013 Feb;71(2):393-7. doi: 10.1016/j.joms.2012.04.031. Epub 2012 Jul 4.

PMID:
22766383
[PubMed - indexed for MEDLINE]
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