Dorothée Reboul

Monosomal karyotype routinely defines a poor prognosis subgroup in acute myeloid leukemia and is frequently associated with TP53 deletion

T. Lavabre‐Bertrand, E. Jourdan, J. Chiésa, 2012, Leukemia & lymphoma.

Comparative evaluation of hepatitis C virus RNA quantitation by branched DNA, NASBA, and monitor assays

J. Piette, J. Huraux, L. Frangeul, 1999, Hepatology.

A homozygous PAX3 mutation leading to severe presentation of Waardenburg syndrome with a prenatal diagnosis

J. Chiésa, F. Grosjean, V. Pingault, 2015, Prenatal diagnosis.

Exon 7 Deletion in the bcr-abl Gene Is Frequent in Chronic Myeloid Leukemia Patients and Is Not Correlated with Resistance against Imatinib

T. Lavabre‐Bertrand, E. Jourdan, J. Chiésa, 2010, Molecular Cancer Therapeutics.

Deletion in the bcr-abl Gene Is Frequent in Chronic loid Leukemia Patients and Is Not Correlated Ther Resistance against Imatinib

T. Lavabre‐Bertrand, J. Chiésa, S. Bravo, 2010 .

OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum

L. Bouneau, C. Rooryck, Angèle Tingaud-Sequeira, 2022, Journal of Medical Genetics.