215 related articles for article (PubMed ID: 17651128)
1. Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia).
Hartsfield JK
Orthod Craniofac Res; 2007 Aug; 10(3):121-8. PubMed ID: 17651128
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid artery.
Legius E; Hellemans M; Wilms G; Tillemans B; Fryns JP
Genet Couns; 1993; 4(4):325-8. PubMed ID: 8110422
[TBL] [Abstract][Full Text] [Related]
4. Oculo-auriculo-vertebral spectrum: clinical and molecular analysis of 51 patients.
Beleza-Meireles A; Hart R; Clayton-Smith J; Oliveira R; Reis CF; Venâncio M; Ramos F; Sá J; Ramos L; Cunha E; Pires LM; Carreira IM; Scholey R; Wright R; Urquhart JE; Briggs TA; Kerr B; Kingston H; Metcalfe K; Donnai D; Newman WG; Saraiva JM; Tassabehji M
Eur J Med Genet; 2015 Sep; 58(9):455-65. PubMed ID: 26206081
[TBL] [Abstract][Full Text] [Related]
5. [The etiology research progress of oculo-auriculo-vertebral spectrum].
Wang P; Fan Y; Chen X
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Dec; 29(24):2184-8. PubMed ID: 27093828
[TBL] [Abstract][Full Text] [Related]
6. Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification.
Tasse C; Böhringer S; Fischer S; Lüdecke HJ; Albrecht B; Horn D; Janecke A; Kling R; König R; Lorenz B; Majewski F; Maeyens E; Meinecke P; Mitulla B; Mohr C; Preischl M; Umstadt H; Kohlhase J; Gillessen-Kaesbach G; Wieczorek D
Eur J Med Genet; 2005; 48(4):397-411. PubMed ID: 16378924
[TBL] [Abstract][Full Text] [Related]
7. Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome.
Kelberman D; Tyson J; Chandler DC; McInerney AM; Slee J; Albert D; Aymat A; Botma M; Calvert M; Goldblatt J; Haan EA; Laing NG; Lim J; Malcolm S; Singer SL; Winter RM; Bitner-Glindzicz M
Hum Genet; 2001 Dec; 109(6):638-45. PubMed ID: 11810276
[TBL] [Abstract][Full Text] [Related]
8. Familial hemifacial microsomia.
Taysi K; Marsh JL; Wise DM
Cleft Palate J; 1983 Jan; 20(1):47-53. PubMed ID: 6572575
[TBL] [Abstract][Full Text] [Related]
9. Hemifacial microsomia and variants: pedigree data.
Rollnick BR; Kaye CI
Am J Med Genet; 1983 Jun; 15(2):233-53. PubMed ID: 6881197
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Candidate genes of oculo-auriculo-vertebral spectrum in 22q region: A systematic review.
Glaeser AB; Santos AS; Diniz BL; Deconte D; Rosa RFM; Zen PRG
Am J Med Genet A; 2020 Nov; 182(11):2624-2631. PubMed ID: 32893956
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 18000524
[TBL] [Abstract][Full Text] [Related]
13. Thrombophilia gene mutations in oculoauriculovertebral spectrum.
Tug E; Atasoy HI; Koybasi Sanal S
Genet Couns; 2012; 23(1):65-72. PubMed ID: 22611644
[TBL] [Abstract][Full Text] [Related]
14. Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS).
Guida V; Calzari L; Fadda MT; Piceci-Sparascio F; Digilio MC; Bernardini L; Brancati F; Mattina T; Melis D; Forzano F; Briuglia S; Mazza T; Bianca S; Valente EM; Salehi LB; Prontera P; Pagnoni M; Tenconi R; Dallapiccola B; Iannetti G; Corsaro L; De Luca A; Gentilini D
Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33530447
[TBL] [Abstract][Full Text] [Related]
15. Distal deletion at 22q11.2 as differential diagnosis in Craniofacial Microsomia: Case report and literature review.
Spineli-Silva S; Bispo LM; Gil-da-Silva-Lopes VL; Vieira TP
Eur J Med Genet; 2018 May; 61(5):262-268. PubMed ID: 29288792
[TBL] [Abstract][Full Text] [Related]
16. Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism.
Van Meter TD; Weaver DD
Clin Dysmorphol; 1996 Jul; 5(3):187-96. PubMed ID: 8818446
[TBL] [Abstract][Full Text] [Related]
17. Craniofacial features in Goldenhar syndrome.
Vinay C; Reddy RS; Uloopi KS; Madhuri V; Sekhar RC
J Indian Soc Pedod Prev Dent; 2009; 27(2):121-4. PubMed ID: 19736507
[TBL] [Abstract][Full Text] [Related]
18. Cranial Nerve Abnormalities in Oculo-Auriculo-Vertebral Spectrum.
Manara R; Brotto D; Ghiselli S; Mardari R; Toldo I; Schifano G; Cantone E; Bovo R; Martini A
AJNR Am J Neuroradiol; 2015 Jul; 36(7):1375-80. PubMed ID: 25814660
[TBL] [Abstract][Full Text] [Related]
19. A family with autosomal dominant oculo-auriculo-vertebral spectrum.
Tasse C; Majewski F; Böhringer S; Fischer S; Lüdecke HJ; Gillessen-Kaesbach G; Wieczorek D
Clin Dysmorphol; 2007 Jan; 16(1):1-7. PubMed ID: 17159507
[TBL] [Abstract][Full Text] [Related]
20. Hemifacial microsomia.
Salvado A; Rodriguez K; Guarisco JL
J La State Med Soc; 2003; 155(3):136-41. PubMed ID: 12873098
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]