APA

Hoffbuhr K., Devaney J. M., LaFleur B., Sirianni N., Scacheri C., Giron J., Schuette J., Innis J., Marino M., Philippart M., Narayanan V., Umansky R., Kronn D., Hoffman E. P. & Naidu S. (20010712). MeCP2 mutations in children with and without the phenotype of Rett syndrome. : Neurology.

Chicago

Hoffbuhr K, Devaney J M, LaFleur B, Sirianni N, Scacheri C, Giron J, Schuette J, Innis J, Marino M, Philippart M, Narayanan V, Umansky R, Kronn D, Hoffman E P and Naidu S. 20010712. MeCP2 mutations in children with and without the phenotype of Rett syndrome. : Neurology.

Harvard

Hoffbuhr K., Devaney J. M., LaFleur B., Sirianni N., Scacheri C., Giron J., Schuette J., Innis J., Marino M., Philippart M., Narayanan V., Umansky R., Kronn D., Hoffman E. P. and Naidu S. (20010712). MeCP2 mutations in children with and without the phenotype of Rett syndrome. : Neurology.

MLA

Hoffbuhr K, Devaney J M, LaFleur B, Sirianni N, Scacheri C, Giron J, Schuette J, Innis J, Marino M, Philippart M, Narayanan V, Umansky R, Kronn D, Hoffman E P and Naidu S. MeCP2 mutations in children with and without the phenotype of Rett syndrome. : Neurology. 20010712.