E. Colin Et Al. , "Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome," AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.6, pp.637-648, 2014
Colin, E. Et Al. 2014. Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.6 , 637-648.
Colin, E., Cong, E. H., Mollet, G., Guichet, A., Gribouval, O., Arrondel, C., ... Boyer, O.(2014). Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.6, 637-648.
Colin, Estelle Et Al. "Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome," AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.6, 637-648, 2014
Colin, Estelle Et Al. "Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome." AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.6, pp.637-648, 2014
Colin, E. Et Al. (2014) . "Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome." AMERICAN JOURNAL OF HUMAN GENETICS , vol.95, no.6, pp.637-648.
@article{article, author={Estelle Colin Et Al. }, title={Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2014, pages={637-648} }