PITX2 and FOXC1 spectrum of mutations in ocular syndromes.
Reis LM; Tyler RC; Volkmann Kloss BA; Schilter KF; Levin AV; Lowry RB; Zwijnenburg PJ; Stroh E; Broeckel U; Murray JC; Semina EV; European Journal Of Human Genetics: EJHG, 2012, vol. 20, issue 12, p 1224, ISSN 14765438. ISBN 14765438.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef