APA

Ehret J. K., Engels H., Cremer K., Becker J., Zimmermann J. P., Wohlleber E., Grasshoff U., Rossier E., Bonin M., Mangold E., Bevot A., Schön S., Heilmann-Heimbach S., Dennert N., Mathieu-Dramard M., Lacaze E., Plessis G., de Broca A., Jedraszak G., Röthlisberger B., Miny P., Filges I., Dufke A., Andrieux J., Lee J. A. & Zink A. M. (20150930). Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. : Molecular cytogenetics.

Chicago

Ehret Julia K, Engels Hartmut, Cremer Kirsten, Becker Jessica, Zimmermann Johannes P, Wohlleber Eva, Grasshoff Ute, Rossier Eva, Bonin Michael, Mangold Elisabeth, Bevot Andrea, Schön Stefanie, Heilmann-Heimbach Stefanie, Dennert Nicola, Mathieu-Dramard Michèle, Lacaze Elodie, Plessis Ghislaine, de Broca Alain, Jedraszak Guillaume, Röthlisberger Benno, Miny Peter, Filges Isabel, Dufke Andreas, Andrieux Joris, Lee Jennifer A and Zink Alexander M. 20150930. Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. : Molecular cytogenetics.

Harvard

Ehret J. K., Engels H., Cremer K., Becker J., Zimmermann J. P., Wohlleber E., Grasshoff U., Rossier E., Bonin M., Mangold E., Bevot A., Schön S., Heilmann-Heimbach S., Dennert N., Mathieu-Dramard M., Lacaze E., Plessis G., de Broca A., Jedraszak G., Röthlisberger B., Miny P., Filges I., Dufke A., Andrieux J., Lee J. A. and Zink A. M. (20150930). Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. : Molecular cytogenetics.

MLA

Ehret Julia K, Engels Hartmut, Cremer Kirsten, Becker Jessica, Zimmermann Johannes P, Wohlleber Eva, Grasshoff Ute, Rossier Eva, Bonin Michael, Mangold Elisabeth, Bevot Andrea, Schön Stefanie, Heilmann-Heimbach Stefanie, Dennert Nicola, Mathieu-Dramard Michèle, Lacaze Elodie, Plessis Ghislaine, de Broca Alain, Jedraszak Guillaume, Röthlisberger Benno, Miny Peter, Filges Isabel, Dufke Andreas, Andrieux Joris, Lee Jennifer A and Zink Alexander M. Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?. : Molecular cytogenetics. 20150930.