APA

Thomas F. P., Geller T. J., Hahn A. F., Gutmann L., Huang X., Wu H., Wyandt H. E. & Lebo R. V. (1999). Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy. : Annals of the New York Academy of Sciences.

Chicago

Thomas Florian P, Geller Thomas J, Hahn Angelika F, Gutmann Ludwig, Huang Xin-Li, Wu Hui, Wyandt Herman E and Lebo Roger V. 1999. Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy. : Annals of the New York Academy of Sciences.

Harvard

Thomas F. P., Geller T. J., Hahn A. F., Gutmann L., Huang X., Wu H., Wyandt H. E. and Lebo R. V. (1999). Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy. : Annals of the New York Academy of Sciences.

MLA

Thomas Florian P, Geller Thomas J, Hahn Angelika F, Gutmann Ludwig, Huang Xin-Li, Wu Hui, Wyandt Herman E and Lebo Roger V. Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy. : Annals of the New York Academy of Sciences. 1999.