Publikationen von 0000-0002-6236-338X
(ORCID: 0000-0002-6236-338X)

Amyere, Mustapha, Vogt, Thomas, Hoo, Joe, Brandrup, Flemming, Bygum, Anette , Boon, Laurence und Vikkula, Miikka (2011) KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation. Journal of Investigative Dermatology 131 (6), S. 1234-1239. Volltext nicht vorhanden.

de Lima, Renata L. L. Ferreira, Hoper, Sarah A., Ghassibe, Michella, Cooper, Margaret E., Rorick, Nicholas K., Kondo, Shinji, Katz, Lori, Marazita, Mary L., Compton, John, Bale, Sherri, Hehr, Ute, Dixon, Michael J., Daack-Hirsch, Sandra , Boute, Odile, Bayet, Bénédicte, Revencu, Nicole, Verellen-Dumoulin, Christine, Vikkula, Miikka , Richieri-Costa, Antônio, Moretti-Ferreira, Danilo , Murray, Jeffrey C. und Schutte, Brian C. (2009) Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome. Genetics in Medicine 11 (4), S. 241-247. Volltext nicht vorhanden.

Zanardo, Livia, Stolz, Wilhelm, Schmitz, Gerd, Kaminski, Wolfgang, Vikkula, Miikka , Landthaler, Michael und Vogt, Thomas (2003) Progressive Hyperpigmentation and Generalized Lentiginosis without Associated Systemic Symptoms: a Rare Hereditary Pigmentation Disorder in South-East Germany. Acta Dermato-Venereologica 84 (1), S. 57-60. Volltext nicht vorhanden.