PITX2 and FOXC1 spectrum of mutations in ocular syndromes

L.M. Reis, R.C. Tyler, B.A.V. Kloss, K.F. Schilter, A.V. Levin, R.B. Lowry, P.J.G. Zwijnenburg, E. Stroh, U. Broeckel, J.C. Murray, E.V. Semina

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)1224-1233
JournalEuropean Journal of Human Genetics
Volume20
Issue number12
DOIs
Publication statusPublished - 2012

Cite this

Reis, L. M., Tyler, R. C., Kloss, B. A. V., Schilter, K. F., Levin, A. V., Lowry, R. B., ... Semina, E. V. (2012). PITX2 and FOXC1 spectrum of mutations in ocular syndromes. European Journal of Human Genetics, 20(12), 1224-1233. https://doi.org/10.1038/ejhg.2012.80