145 related articles for article (PubMed ID: 1583660)
21. 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. PubMed ID: 18019368
[TBL] [Abstract][Full Text] [Related]
22. Facial asymmetry quantitative evaluation in oculoauriculovertebral spectrum.
Manara R; Schifano G; Brotto D; Mardari R; Ghiselli S; Gerunda A; Ghirotto C; Fusetti S; Piacentile K; Scienza R; Ermani M; Martini A
Clin Oral Investig; 2016 Mar; 20(2):219-25. PubMed ID: 26578120
[TBL] [Abstract][Full Text] [Related]
23. Precocious puberty in a patient with Oculo-Auriculo-Verebral spectrum (OAVS).
Berio A; Garlaschi G; Piazzi A
Pediatr Med Chir; 2014 Jun; 36(3):11. PubMed ID: 25573646
[TBL] [Abstract][Full Text] [Related]
24. Diencephalic neuronal hamartoma associated with congenital obstructive hydrocephalus, anophthalmia, cleft lip and palate and severe mental retardation: a possible new syndrome.
Rossiter JP; Khalifa MM; Nag S
Acta Neuropathol; 2000 Jun; 99(6):685-90. PubMed ID: 10867803
[TBL] [Abstract][Full Text] [Related]
25. Abnormal soft palate movements in patients with microtia.
Kolodzynski MN; van Hoorn BT; Kon M; Breugem CC
J Plast Reconstr Aesthet Surg; 2018 Oct; 71(10):1476-1480. PubMed ID: 30001915
[TBL] [Abstract][Full Text] [Related]
26. 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. PubMed ID: 19111916
[TBL] [Abstract][Full Text] [Related]
27. Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum.
Güleray N; Koşukcu C; Oğuz S; Ürel Demir G; Taşkıran EZ; Kiper PÖŞ; Utine GE; Alanay Y; Boduroğlu K; Alikaşifoğlu M
Cleft Palate Craniofac J; 2022 Sep; 59(9):1114-1124. PubMed ID: 34410171
[TBL] [Abstract][Full Text] [Related]
28. [Goldenhar syndrome. Report of a new case].
Pedraz García C; Benito Zaballos MF; García González P; Carbajosa Herrero T; Heras de Pedro M; Santos Borbujo J; Gil Sánchez A; Salazar Villalobos V
An Esp Pediatr; 1984 Mar; 20(4):403-7. PubMed ID: 6732067
[TBL] [Abstract][Full Text] [Related]
29. Bilateral microtia with severe cardiac defect: a new syndrome, or a severe manifestation of the oculoauriculovertebral spectrum?
McKee S; Mabrouk R; Bali S
Clin Dysmorphol; 2006 Apr; 15(2):121-2. PubMed ID: 16531742
[TBL] [Abstract][Full Text] [Related]
30. Oculoauriculovertebral spectrum and maxillary sinus volumes : CT-based comparative evaluation.
Hofmann E; Detterbeck A; Chepura T; Kirschneck C; Schmid M; Hirschfelder U
J Orofac Orthop; 2018 Jul; 79(4):259-266. PubMed ID: 29947815
[TBL] [Abstract][Full Text] [Related]
31. Three-dimensional CT evaluation of oculoauriculovertebral spectrum patients use of Katsumata's asymmetry index.
Hofmann E; Schmid M; Steinhäuser-Andresen S; Hirschfelder U
J Orofac Orthop; 2016 May; 77(3):176-84. PubMed ID: 27103014
[TBL] [Abstract][Full Text] [Related]
32. Clinical and cytogenetic features of a Brazilian sample of patients with phenotype of oculo-auriculo-vertebral spectrum: a cross-sectional study.
Silva AP; Rosa RF; Trevisan P; Dorneles JC; Mesquita CS; Mattos VF; Paskulin GA; Zen PR
Sao Paulo Med J; 2015; 133(3):191-8. PubMed ID: 25337663
[TBL] [Abstract][Full Text] [Related]
33. Severe oculocerebrocutaneous (Delleman) syndrome: overlap with Goldenhar anomaly.
McCandless SE; Robin NH
Am J Med Genet; 1998 Jul; 78(3):282-5. PubMed ID: 9677067
[TBL] [Abstract][Full Text] [Related]
34. Congenital ameloblastic fibroma in association with oculoauriculovertebral spectrum.
Naidoo LC; Stephen LX
Int J Pediatr Otorhinolaryngol; 1998 May; 43(3):283-8. PubMed ID: 9663951
[TBL] [Abstract][Full Text] [Related]
35. Clinical and cytogenomic findings in OAV spectrum.
Bragagnolo S; Colovati MES; Souza MZ; Dantas AG; F de Soares MF; Melaragno MI; Perez AB
Am J Med Genet A; 2018 Mar; 176(3):638-648. PubMed ID: 29368383
[TBL] [Abstract][Full Text] [Related]
36. An interesting case presentation: pulmonary malformations associated with oculoauriculovertebral dysplasia (Goldenhar anomalad).
Downing GJ; Kilbride H
J Perinatol; 1991 Jun; 11(2):190-2. PubMed ID: 1890482
[TBL] [Abstract][Full Text] [Related]
37. Functional and genetic analyses of ZYG11B provide evidences for its involvement in OAVS.
Tingaud-Sequeira A; Trimouille A; Marlin S; Lopez E; Berenguer M; Gherbi S; Arveiler B; Lacombe D; Rooryck C
Mol Genet Genomic Med; 2020 Oct; 8(10):e1375. PubMed ID: 32738032
[TBL] [Abstract][Full Text] [Related]
38.
Celse T; Tingaud-Sequeira A; Dieterich K; Siegfried G; Lecaignec C; Bouneau L; Fannemel M; Salaun G; Laffargue F; Martinez G; Satre V; Vieville G; Bidart M; Soussi Zander C; Turesson AC; Splitt M; Reboul D; Chiesa J; Khau Van Kien P; Godin M; Gruchy N; Goel H; Palmer E; Demetriou K; Shalhoub C; Rooryck C; Coutton C
J Med Genet; 2023 Jun; 60(6):620-626. PubMed ID: 36368868
[TBL] [Abstract][Full Text] [Related]
39. Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement.
Ou Z; Martin DM; Bedoyan JK; Cooper ML; Chinault AC; Stankiewicz P; Cheung SW
Am J Med Genet A; 2008 Oct; 146A(19):2480-9. PubMed ID: 18666230
[TBL] [Abstract][Full Text] [Related]
40. Early prenatal diagnosis of oculoauriculovertebral dysplasia or the Goldenhar syndrome.
De Catte L; Laubach M; Legein J; Goossens A
Ultrasound Obstet Gynecol; 1996 Dec; 8(6):422-4. PubMed ID: 9014284
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]