APA

Zink A. M., Wohlleber E., Engels H., Rødningen O. K., Ravn K., Heilmann S., Rehnitz J., Katzorke N., Kraus C., Blichfeldt S., Hoffmann P., Reutter H., Brockschmidt F. F., Kreiß-Nachtsheim M., Vogt P. H., Prescott T. E., Tümer Z. & Lee J. A. (20140409). Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies. : Molecular syndromology.

Chicago

Zink A M, Wohlleber E, Engels H, Rødningen O K, Ravn K, Heilmann S, Rehnitz J, Katzorke N, Kraus C, Blichfeldt S, Hoffmann P, Reutter H, Brockschmidt F F, Kreiß-Nachtsheim M, Vogt P H, Prescott T E, Tümer Z and Lee J A. 20140409. Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies. : Molecular syndromology.

Harvard

Zink A. M., Wohlleber E., Engels H., Rødningen O. K., Ravn K., Heilmann S., Rehnitz J., Katzorke N., Kraus C., Blichfeldt S., Hoffmann P., Reutter H., Brockschmidt F. F., Kreiß-Nachtsheim M., Vogt P. H., Prescott T. E., Tümer Z. and Lee J. A. (20140409). Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies. : Molecular syndromology.

MLA

Zink A M, Wohlleber E, Engels H, Rødningen O K, Ravn K, Heilmann S, Rehnitz J, Katzorke N, Kraus C, Blichfeldt S, Hoffmann P, Reutter H, Brockschmidt F F, Kreiß-Nachtsheim M, Vogt P H, Prescott T E, Tümer Z and Lee J A. Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies. : Molecular syndromology. 20140409.