Number of items: 2.
2011
Krumbiegel, M.,
Pasutto, F.,
Schlötzer-Schrehardt, U.,
Uebe, S.,
Zenkel, M.,
Mardin, C. Y.,
Weisschuh, N.,
Paoli, D.,
Gramer, E.,
Becker, C.,
Ekici, A. B.,
Weber, Bernhard H. F. ,
Nürnberg, P.,
Kruse, F. E. and
Reis, A.
(2011)
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.
European Journal of Human Genetics 19 (2), pp. 186-193.
Fulltext not available.
2009
Krumbiegel, M.,
Pasutto, F.,
Mardin, C. Y.,
Weisschuh, N.,
Paoli, D.,
Gramer, E.,
Zenkel, M.,
Weber, Bernhard H. F. ,
Kruse, F. E.,
Schlötzer-Schrehardt, U. and
Reis, A.
(2009)
Exploring functional candidate genes for genetic association in German patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.
Investigative ophthalmology and visual science 50 (6), pp. 2796-2801.
This list was generated on Mon Dec 9 23:17:23 2024 CET.