Hussain, M., Baig, S., Neumann, S., Nürnberg, G., Farooq, M., Ahmad, I., . . . Nürnberg, P. (2012). A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function. Elsevier.
Stile di citazione ChicagoHussain, Muhammad Sajid, et al. A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function. Elsevier, 2012.
Citazione MLAHussain, Muhammad Sajid, et al. A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function. Elsevier, 2012.
Attenzione: Queste citazioni potrebbero non essere precise al 100%.