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Leukemia|November 1, 1992
Relapse as acute monoblastic leukemia (AML-M5) of t(6;9) acute myeloblastic leukemia (AML-M2)R Berger, M T Daniel, P Jonveaux, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1991
Lack of mutations in the TP53 tumor suppressor gene exons 5 to 8 in Fanconi's anemiaP Jonveaux, M Le Coniat, D Grausz, et al.Leukemia & Lymphoma|May 1, 1995
Trisomy 14: a recurring cytogenetic abnormality associated with myeloid disordersH Poirel, P Jonveaux, M T Daniel, et al.Familial Cancer|March 19, 2018
Clinical and pathologic characteristics of breast cancer patients carrying the c.3481_3491del11 mutationR El Tannouri, E Albuisson, P Jonveaux, et al.Cancer Genetics and Cytogenetics|March 1, 1994
Cytogenetic studies in patients with Richter's syndromeJ Hébert, P Jonveaux, M F d'Agay, et al.Hematology and Cell Therapy|April 1, 1996
Secondary acute myeloblastic leukemia with t(16;21) (q24;q22). involving the AML1 geneR Berger, M Le Coniat, S P Romana, et al.Annales De Genetique|January 5, 2002
Deletion screening by fluorescence in situ hybridization in Rett syndrome patientsV Bourdon, C Philippe, A Grandemenge, et al.Hematologic Pathology|January 1, 1991
Loss of genetic material from the short arm of chromosome 12 is a frequent secondary abnormality in non-Hodgkin's lymphomaP Jonveaux, M Le Coniat, J Derré, et al.Leukemia|November 1, 1996
Faconi anemia and bone marrow clonal chromosome abnormalitiesO Maarek, P Jonveaux, M Le Coniat, et al.Journal Francais D'Ophtalmologie|June 3, 2011
[Wolfram syndrome: clinical and genetic analysis in two sisters]J-B Conart, T Maalouf, P Jonveaux, et al.Pageof 10