APA

Kriederman B. M., Myloyde T. L., Witte M. H., Dagenais S. L., Witte C. L., Rennels M., Bernas M. J., Lynch M. T., Erickson R. P., Caulder M. S., Miura N., Jackson D., Brooks B. P. & Glover T. W. (20040211). FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. : Human molecular genetics.

Chicago

Kriederman Benjamin M, Myloyde Teressa L, Witte Marlys H, Dagenais Susan L, Witte Charles L, Rennels Margaret, Bernas Michael J, Lynch Michelle T, Erickson Robert P, Caulder Mark S, Miura Naoyuki, Jackson David, Brooks Brian P and Glover Thomas W. 20040211. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. : Human molecular genetics.

Harvard

Kriederman B. M., Myloyde T. L., Witte M. H., Dagenais S. L., Witte C. L., Rennels M., Bernas M. J., Lynch M. T., Erickson R. P., Caulder M. S., Miura N., Jackson D., Brooks B. P. and Glover T. W. (20040211). FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. : Human molecular genetics.

MLA

Kriederman Benjamin M, Myloyde Teressa L, Witte Marlys H, Dagenais Susan L, Witte Charles L, Rennels Margaret, Bernas Michael J, Lynch Michelle T, Erickson Robert P, Caulder Mark S, Miura Naoyuki, Jackson David, Brooks Brian P and Glover Thomas W. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. : Human molecular genetics. 20040211.