APA
Alam N. A., Rowan A. J., Wortham N. C., Pollard P. J., Mitchell M., Tyrer J. P., Barclay E., Calonje E., Manek S., Adams S. J., Bowers P. W., Burrows N. P., Charles-Holmes R., Cook L. J., Daly B. M., Ford G. P., Fuller L. C., Hadfield-Jones S. E., Hardwick N., Highet A. S., Keefe M., MacDonald-Hull S. P., Potts E. D. A., Crone M., Wilkinson S., Camacho-Martinez F., Jablonska S., Ratnavel R., MacDonald A., Mann R. J., Grice K., Guillet G., Lewis-Jones M. S., McGrath H., Seukeran D. C., Morrison P. J., Fleming S., Rahman S., Kelsell D., Leigh I., Olpin S. & Tomlinson I. P. M. (20040130). Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. : Human molecular genetics.
Chicago
Alam N A, Rowan A J, Wortham N C, Pollard P J, Mitchell M, Tyrer J P, Barclay E, Calonje E, Manek S, Adams S J, Bowers P W, Burrows N P, Charles-Holmes R, Cook L J, Daly B M, Ford G P, Fuller L C, Hadfield-Jones S E, Hardwick N, Highet A S, Keefe M, MacDonald-Hull S P, Potts E D A, Crone M, Wilkinson S, Camacho-Martinez F, Jablonska S, Ratnavel R, MacDonald A, Mann R J, Grice K, Guillet G, Lewis-Jones M S, McGrath H, Seukeran D C, Morrison P J, Fleming S, Rahman S, Kelsell D, Leigh I, Olpin S and Tomlinson I P M. 20040130. Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. : Human molecular genetics.
Harvard
Alam N. A., Rowan A. J., Wortham N. C., Pollard P. J., Mitchell M., Tyrer J. P., Barclay E., Calonje E., Manek S., Adams S. J., Bowers P. W., Burrows N. P., Charles-Holmes R., Cook L. J., Daly B. M., Ford G. P., Fuller L. C., Hadfield-Jones S. E., Hardwick N., Highet A. S., Keefe M., MacDonald-Hull S. P., Potts E. D. A., Crone M., Wilkinson S., Camacho-Martinez F., Jablonska S., Ratnavel R., MacDonald A., Mann R. J., Grice K., Guillet G., Lewis-Jones M. S., McGrath H., Seukeran D. C., Morrison P. J., Fleming S., Rahman S., Kelsell D., Leigh I., Olpin S. and Tomlinson I. P. M. (20040130). Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. : Human molecular genetics.
MLA
Alam N A, Rowan A J, Wortham N C, Pollard P J, Mitchell M, Tyrer J P, Barclay E, Calonje E, Manek S, Adams S J, Bowers P W, Burrows N P, Charles-Holmes R, Cook L J, Daly B M, Ford G P, Fuller L C, Hadfield-Jones S E, Hardwick N, Highet A S, Keefe M, MacDonald-Hull S P, Potts E D A, Crone M, Wilkinson S, Camacho-Martinez F, Jablonska S, Ratnavel R, MacDonald A, Mann R J, Grice K, Guillet G, Lewis-Jones M S, McGrath H, Seukeran D C, Morrison P J, Fleming S, Rahman S, Kelsell D, Leigh I, Olpin S and Tomlinson I P M. Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. : Human molecular genetics. 20040130.