|1.||Zarbalis, Konstantinos S: 1 article (01/2014)|
|2.||Ross, Adam P: 1 article (01/2014)|
|3.||McParland, Joanna: 1 article (07/2012)|
|4.||Oldridge, Michael: 1 article (07/2012)|
|5.||Lester, Tracy: 1 article (07/2012)|
|6.||Archer, Caroline: 1 article (07/2012)|
|7.||O'Rourke, Anthony: 1 article (07/2012)|
|8.||Seller, Anneke: 1 article (07/2012)|
|9.||Brekelmans, Roel: 1 article (07/2012)|
|10.||Bowman, Michael: 1 article (07/2012)|
|1.||Goldenhar Syndrome (Syndrome, Oculoauriculovertebral)
05/01/2009 - "Systemic associations included Goldenhar syndrome and Treacher-Collins-Franceschetti syndrome. "
04/01/2005 - "After the identification of mutations in TCOF1 as a general cause of the Treacher-Collins-Franceschetti syndrome, TCOF1 mutations were excluded in patients with unilateral signs of the Goldenhar syndrome spectrum. "
04/01/2005 - "A number of different disorders involving first and second branchial arch anomalies have been described as distinct entities, including Treacher-Collins-Franceschetti syndrome, Goldenhar syndrome, Nager syndrome and Miller syndrome. "
|2.||Hearing Loss (Hearing Impairment)
|3.||Diamond-Blackfan Anemia (Anemia, Diamond Blackfan)
01/01/2014 - "This review explores the particular importance of ribosome biogenesis defects in this context since a specific interface between ribosomopathies and neurocristopathies exists as evidenced by disorders such as Treacher-Collins-Franceschetti syndrome (TCS) and Diamond-Blackfan anemia (DBA). "
|2.||Genetic Markers (Genetic Marker)
|3.||Nager type Acrofacial dysostosis