167 related articles for article (PubMed ID: 16761296)
41. Two neighboring microdeletions of 5q13.2 in a child with oculo-auriculo-vertebral spectrum.
Huang XS; Xiao L; Li X; Xie Y; Jiang HO; Tan C; Wang L; Zhang JX
Eur J Med Genet; 2010; 53(3):153-8. PubMed ID: 20346424
[TBL] [Abstract][Full Text] [Related]
42. Oculo-auriculo-vertebral spectrum: new genes and literature review on a complex disease.
Tingaud-Sequeira A; Trimouille A; Sagardoy T; Lacombe D; Rooryck C
J Med Genet; 2022 May; 59(5):417-427. PubMed ID: 35110414
[TBL] [Abstract][Full Text] [Related]
43. Microtia: a clinical and genetic study at the National Institute of Pediatrics in Mexico City.
Llano-Rivas I; González-del Angel A; del Castillo V; Reyes R; Carnevale A
Arch Med Res; 1999; 30(2):120-4. PubMed ID: 10372445
[TBL] [Abstract][Full Text] [Related]
44. Ultrasound diagnosis of oculo-auriculo-vertebral spectrum in a mid-trimester foetus.
Song QY; Luo H
Prenat Diagn; 2021 May; 41(6):791-792. PubMed ID: 33991116
[No Abstract] [Full Text] [Related]
45. Oculo-auriculo-vertebral (Goldenhar) spectrum associated with pericentric inversion 9: coincidental findings or etiologic factor?
Stanojević M; Stipoljev F; Koprcina B; Kurjak A
J Craniofac Genet Dev Biol; 2000; 20(3):150-4. PubMed ID: 11321600
[TBL] [Abstract][Full Text] [Related]
46. Prenatal diagnosis of Goldenhar syndrome with unusual features by 3D ultrasonography.
Guzelmansur I; Ceylaner G; Ceylaner S; Ceylan N; Daplan T
Genet Couns; 2013; 24(3):319-25. PubMed ID: 24341148
[TBL] [Abstract][Full Text] [Related]
47. Oculo-auriculo-vertebral spectrum, cat eye, and distal 22q11 microdeletion syndromes: a unique double rearrangement.
Torti EE; Braddock SR; Bernreuter K; Batanian JR
Am J Med Genet A; 2013 Aug; 161A(8):1992-8. PubMed ID: 23894059
[TBL] [Abstract][Full Text] [Related]
48. Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature.
Vendramini S; Richieri-Costa A; Guion-Almeida ML
Eur J Hum Genet; 2007 Apr; 15(4):411-21. PubMed ID: 17290277
[TBL] [Abstract][Full Text] [Related]
49. [Oculo-auriculo-vertebral spectrum in patients with congenital heart defects].
Rosa RF; Zen PR; Flores JA; Golendziner E; Pilla CB; Roman T; Varella-Garcia M; Paskulin GA
Arq Bras Cardiol; 2010 Oct; 95(4):436-9. PubMed ID: 20802965
[TBL] [Abstract][Full Text] [Related]
50. Characterization of facial paresis in hemifacial microsomia.
Cline JM; Hicks KE; Patel KG
Otolaryngol Head Neck Surg; 2014 Feb; 150(2):188-93. PubMed ID: 24492209
[TBL] [Abstract][Full Text] [Related]
51. Encephalocele-radial, cardiac, gastrointestinal, anal/renal anomalies: novel evidence for a new condition?
Valdez CM; Altmayer SP; Barrow MA; Telles JA; Betat Rda S; Zen PR; Rosa RF
Am J Med Genet A; 2014 May; 164A(5):1085-91. PubMed ID: 24648351
[TBL] [Abstract][Full Text] [Related]
52. Goldenhar syndrome (oculo-auriculo-vertebral spectrum): Findings on cone beam computed tomography-3 case reports.
Maryanchik I; Nair MK
Oral Surg Oral Med Oral Pathol Oral Radiol; 2018 Oct; 126(4):e233-e239. PubMed ID: 29857980
[TBL] [Abstract][Full Text] [Related]
53. Association of segmental neurofibromatosis 1 and oculo-auriculo-vertebral spectrum in a 24-year-old female.
Castori M; Majore S; Romanelli F; Didona B; Grammatico P; Zambruno G
Eur J Dermatol; 2008; 18(1):22-5. PubMed ID: 18086584
[TBL] [Abstract][Full Text] [Related]
54. 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]
55. Proposed clinical approach and imaging studies in families with oculo-auriculo-vertebral spectrum to assess variable expressivity.
Estandia-Ortega B; Fernández-Hernández L; Alcántara-Ortigoza MA; González-Del Angel A
Am J Med Genet A; 2022 May; 188(5):1515-1525. PubMed ID: 35119197
[TBL] [Abstract][Full Text] [Related]
56. An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases.
Vendramini-Pittoli S; Guion-Almeida ML; Santos JM; Garcia Júnior SM; Yoshida MM; Richieri-Costa A; Kokitsu-Nakata NM
Clin Dysmorphol; 2015 Oct; 24(4):144-50. PubMed ID: 25816358
[TBL] [Abstract][Full Text] [Related]
57. Oculo-auriculo-vertebral spectrum (OAVS) with large cerebral cyst: affinity to holoprosencephaly.
Berio A; Mangiante G; Oliaro E; Piazzi A
Minerva Pediatr; 2012 Oct; 64(5):549-55. PubMed ID: 22992537
[No Abstract] [Full Text] [Related]
58. Reproduction abnormalities and twin pregnancies in parents of sporadic patients with oculo-auriculo-vertebral spectrum/Goldenhar syndrome.
Wieczorek D; Ludwig M; Boehringer S; Jongbloet PH; Gillessen-Kaesbach G; Horsthemke B
Hum Genet; 2007 May; 121(3-4):369-76. PubMed ID: 17297623
[TBL] [Abstract][Full Text] [Related]
59. Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum Phenotype.
Colovati ME; Bragagnolo S; Guilherme RS; Dantas AG; Soares MF; Kim CA; Perez AB; Melaragno MI
Cytogenet Genome Res; 2015; 147(2-3):130-4. PubMed ID: 26919065
[TBL] [Abstract][Full Text] [Related]
60. Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanisms.
Zamariolli M; Burssed B; Moysés-Oliveira M; Colovati M; Bellucco FTDS; Dos Santos LC; Alvarez Perez AB; Bragagnolo S; Melaragno MI
Am J Med Genet A; 2021 Jul; 185(7):2056-2064. PubMed ID: 33880880
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]