Farag, H. G., Froehler, S., Oexle, K., Ravindran, E., Schindler, D., Staab, T., . . . Kaindl, A. M. (2013). Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. Orphanet J Rare Dis.
Dyfyniad Arddull ChicagoFarag, Heba Gamal, et al. "Abnormal Centrosome and Spindle Morphology in a Patient With Autosomal Recessive Primary Microcephaly Type 2 Due to Compound Heterozygous WDR62 Gene Mutation." Orphanet J Rare Dis 2013.
Dyfyniad MLAFarag, Heba Gamal, et al. "Abnormal Centrosome and Spindle Morphology in a Patient With Autosomal Recessive Primary Microcephaly Type 2 Due to Compound Heterozygous WDR62 Gene Mutation." Orphanet J Rare Dis 2013.