APA

McConkie-Rosell A., Lachiewicz A. M., Spiridigliozzi G. A., Tarleton J., Schoenwald S., Phelan M. C., Goonewardena P., Ding X. & Brown W. T. (19931028). Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. : American journal of human genetics.

Chicago

McConkie-Rosell A, Lachiewicz A M, Spiridigliozzi G A, Tarleton J, Schoenwald S, Phelan M C, Goonewardena P, Ding X and Brown W T. 19931028. Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. : American journal of human genetics.

Harvard

McConkie-Rosell A., Lachiewicz A. M., Spiridigliozzi G. A., Tarleton J., Schoenwald S., Phelan M. C., Goonewardena P., Ding X. and Brown W. T. (19931028). Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. : American journal of human genetics.

MLA

McConkie-Rosell A, Lachiewicz A M, Spiridigliozzi G A, Tarleton J, Schoenwald S, Phelan M C, Goonewardena P, Ding X and Brown W T. Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. : American journal of human genetics. 19931028.