APA

Farag H. G., Froehler S., Oexle K., Ravindran E., Schindler D., Staab T., Huebner A., Kraemer N., Chen W. & Kaindl A. M. (20140717). Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. : Orphanet journal of rare diseases.

Chicago

Farag Heba Gamal, Froehler Sebastian, Oexle Konrad, Ravindran Ethiraj, Schindler Detlev, Staab Timo, Huebner Angela, Kraemer Nadine, Chen Wei and Kaindl Angela M. 20140717. Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. : Orphanet journal of rare diseases.

Harvard

Farag H. G., Froehler S., Oexle K., Ravindran E., Schindler D., Staab T., Huebner A., Kraemer N., Chen W. and Kaindl A. M. (20140717). Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. : Orphanet journal of rare diseases.

MLA

Farag Heba Gamal, Froehler Sebastian, Oexle Konrad, Ravindran Ethiraj, Schindler Detlev, Staab Timo, Huebner Angela, Kraemer Nadine, Chen Wei and Kaindl Angela M. Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. : Orphanet journal of rare diseases. 20140717.