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

113 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)1224-1233
JournalEuropean journal of human genetics
Issue number12
Publication statusPublished - 2012

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