Millot, F. Et Al. 2017. Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents. CANCER , vol.123, no.18 , 3609-3616.

Millot, F., Dupraz, C., Guilhot, J., Suttorp, M., Brizard, F., Leblanc, T., ... Gunes, A.(2017). Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents. CANCER , vol.123, no.18, 3609-3616.

Millot, Frederic Et Al. "Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents," CANCER , vol.123, no.18, 3609-3616, 2017

Millot, Frederic Et Al. "Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents." CANCER , vol.123, no.18, pp.3609-3616, 2017

Millot, F. Et Al. (2017) . "Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents." CANCER , vol.123, no.18, pp.3609-3616.

@article{article, author={Frederic Millot Et Al. }, title={Additional cytogenetic abnormalities and variant t(9;22) at the diagnosis of childhood chronic myeloid leukemia: The experience of the International Registry for Chronic Myeloid Leukemia in Children and Adolescents}, journal={CANCER}, year=2017, pages={3609-3616} }