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Sequencing of the hypoxia pathway genes in patients with congenital erythrocytoses by next generation sequencing

Autor: Girodon, F., Pacault, F., Airaud, M., Garrec, C., Corbineau, S., Casadevall, N., Rose, C., de Renzis, B., Peroni, E., Randi, Ml., Dumont, S., Ricordeau, I., Bezieau, S., Gardie, B.

Publikováno v: Haematologica
22nd Congress of the European Hematology Association
22nd Congress of the European Hematology Association, Jun 2017, Madrid, Spain. pp.P712
22nd Congress of the European Hematology Association, Jun 2017, Madrid, Spain. Haematologica, 102 (S2), pp.P712, 2017, 22nd Congress of the European Hematology Association Madrid, Spain, June 22–25, 2017. 〈http://www.haematologica.org/content/102/s2〉

IF 7.702; International audience

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6f25805ab8af163fba5fc99cf9e4cb5a
https://u-bourgogne.hal.science/hal-01633522