APA

Meijer H., de Graaff E., Merckx D. M., Jongbloed R. J., de Die-Smulders C. E., Engelen J. J., Fryns J. P., Curfs P. M. & Oostra B. A. (19940927). A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome. : Human molecular genetics.

Chicago

Meijer H, de Graaff E, Merckx D M, Jongbloed R J, de Die-Smulders C E, Engelen J J, Fryns J P, Curfs P M and Oostra B A. 19940927. A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome. : Human molecular genetics.

Harvard

Meijer H., de Graaff E., Merckx D. M., Jongbloed R. J., de Die-Smulders C. E., Engelen J. J., Fryns J. P., Curfs P. M. and Oostra B. A. (19940927). A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome. : Human molecular genetics.

MLA

Meijer H, de Graaff E, Merckx D M, Jongbloed R J, de Die-Smulders C E, Engelen J J, Fryns J P, Curfs P M and Oostra B A. A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome. : Human molecular genetics. 19940927.