Cytogénétique des syndromes myélodysplasiques = Cytogenetic of myelodysplastic syndromesLAÏ, J. L; FENAUX, P.Pathologie et biologie. 1997, Vol 45, Num 7, pp 550-555, issn 0369-8114Article

Reassessment of an apparent t(12;17)(p11;p11) as an unbalanced t(17;21)(p11;q11) in a case of B-cell chronic lymphocytic leukemia by fluorescence in situ hybridizationFALCTIF, M; LAÏ, J. L; FENAUX, P et al.Cancer genetics and cytogenetics. 1994, Vol 78, Num 1, pp 108-111, issn 0165-4608Article

Multiple myeloma : Almost all patients are cytogenetically abnormalZANDECKI, M; LAÏ, J.-L; FACON, T et al.British journal of haematology. 1996, Vol 94, Num 2, pp 217-227, issn 0007-1048Article

JAK2V617F-positive polycythemia vera and Philadelphia chromosome-positive chronic myeloid leukemia : one patient with two distinct myeloproliferative disordersCAMBIER, N; RENNEVILLE, A; CAZAENTRE, T et al.Leukemia. 2008, Vol 22, Num 7, pp 1454-1455, issn 0887-6924, 2 p.Article

De novo myelodysplastic syndrome (MDS) with deletion of the long arm of chromosome 20 : a subtype of MDS with distinct hematological and prognostic features ?WATTEL, E; LAÏ, J.-L; MOHAMED HEBBAR et al.Leukemia research. 1993, Vol 17, Num 11, pp 921-926, issn 0145-2126Article

Manifestations cutanées révélatrices d'une leucémie monoblastique = Cutaneous symptoms revealing M5 acute myeloid leukemiaDALLE, J.-H; MORTIER, L; ROUMIER, C et al.Archives de pédiatrie (Paris). 2002, Vol 9, Num 10, pp 1046-1049, issn 0929-693X, 4 p.Article

Hémopathies malignes et translocation t(6;9)(p23;q34), étude cytologique, cytogénétique et moléculaire de quatre cas = Malignant hemopathies and translocations t(6;9) (p23;q34), cytological, cytogenetical and molecular study of four casesROUMIER, C; SOENEN, V; LAÏ, J.-L et al.Hématologie (Montrouge). 1999, Vol 5, Num 6, pp 523-527, issn 1264-7527Article

Chronic myelogenous leukemia with translocation (8; 22): report of a new caseLAÏ, J. L; JOUET, J.-P; BAUTERS, F et al.Cancer genetics and cytogenetics. 1985, Vol 17, Num 4, pp 365-366, issn 0165-4608Article

Investigation of minimal residual disease in adult Ph1 positive acute lymphoblastic leukemia by a combination of cell sorting and fluorescence in situ hybridization : A preliminary study on 6 casesCAMBIER, N; SOENEN-CORNU, V; LAÏ, J.-L et al.Haematologica (Roma). 2000, Vol 85, Num 6, pp 664-665, issn 0390-6078Article

Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea : High proportion of cases with 17p deletionSTERKERS, Y; PREUDHOMME, C; LAÏ, J.-L et al.Blood. 1998, Vol 91, Num 2, pp 616-622, issn 0006-4971Article

Translocation (3;13)(q27;q14) : A nonrandom and probably secondary structural change in non-Hodgkin lymphomasLAÏ, J.-L; DAUDIGNON, A; KERCKAERT, J.-P et al.Cancer genetics and cytogenetics. 1998, Vol 103, Num 2, pp 140-143, issn 0165-4608Article

Evaluation of minimal residual disease by interphase FISH in multiple myeloma : does complete remission exist ?GENEVIEVE, F; ZANDECKI, M; LAÏ, J.-L et al.Leukemia. 1999, Vol 13, Num 4, pp 641-644, issn 0887-6924Article

Four cases of follicular lymphoma with t(14;18)(q32;q21) and t(3;4)(q27;p13) with LAZ3 (BCL6) rearrangementDAUDIGNON, A; BISIAU, H; LE BARON, F et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 2, pp 157-160, issn 0165-4608Article

Transient leukemoid disorder in a newborn with Down syndrome followed 19 months later by an acute myeloid leukemia : Demonstration of the same structural change in both instances with clonal evolutionDUFLOS-DELAPLACE, D; LAÏ, J.-L; NELKEN, B et al.Cancer genetics and cytogenetics. 1999, Vol 113, Num 2, pp 166-171, issn 0165-4608Article

Several cytogenetic subclones may be identified within plasma cells from patients with monoclonal gammopathy of undetermined significance, both at diagnosis and during the indolent course of this conditionZANDECKI, M; LAÏ, J.-L; GENEVIEVE, F et al.Blood. 1997, Vol 90, Num 9, pp 3682-3690, issn 0006-4971Article

17p deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situSOENEN, V; PREUDHOMME, C; ROUMIER, C et al.Blood. 1998, Vol 91, Num 3, pp 1008-1015, issn 0006-4971Article

Les anomalies chromosomiques des lymphomes malins et des tumeurs solides = Chromosomal aberrations in solid tumor and malignant lymphomaCAPPELAERE, P; LAI, J. L.Lille médical (1987). 1989, Vol 29, Num 1, pp 32-40, 9 p.Article

Is there still a role for low-dose cytosine arabinoside in de novo acute myeloid leukemia in the elderly ? A report on 77 casesDETOURMIGNIES, L; WATTEL, E; LAÏ, J. L et al.Annals of hematology (Print). 1993, Vol 66, Num 5, pp 235-240, issn 0939-5555Article

Is translocation (8;21) a favorable cytogenetic rearrangement in acute myeloid leukemia?FENAUX, P; LAÏ, J. L; PREUDHOMME, C et al.Nouvelle revue française d'hématologie. 1990, Vol 32, Num 3, pp 179-182, issn 0029-4810, 4 p.Article

Cytogénétique des hémopathies malignes : actualités = Cytogenetics of malignant hemopathy : updateLAI, J.-L; GENEVIEVE, F; ZANDECKI, M et al.Bulletin du cancer. 1999, Vol 86, Num 1, pp 23-28, issn 0007-4551Article

Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myelomaFLACTIF, M; ZANDECKI, M; LAÏ, J. L et al.Leukemia. 1995, Vol 9, Num 12, pp 2109-2114, issn 0887-6924Article

Image analysis in multiple myeloma at diagnosis : correlation with cytogenetic studyZANDECKI, M; BERNARDI, F; LAÏ, J. L et al.Cancer genetics and cytogenetics. 1994, Vol 74, Num 2, pp 115-119, issn 0165-4608Article

Two cases of t(1:16)(p11;p11) in multiple myeloma : confirmation by chromosome paintingPLACTIF, M; LAÏ, J. L; ZANDECKI, M et al.Cancer genetics and cytogenetics. 1994, Vol 76, Num 1, pp 10-14, issn 0165-4608Article

Involvement of peripheral blood cells in multiple myeloma : chromosome changes are the rule within circulating plasma cells but not within B lymphocytesZANDECKI, M; BERNARDI, F; GENEVIEVE, F et al.Leukemia. 1997, Vol 11, Num 7, pp 1034-1039, issn 0887-6924Article

Cytogenetics in multiple myeloma : A multicenter study of 24 patients with t(11;14)(q13;q32) or its variantLAÏ, J. L; MICHAUX, L; DASTUGUE, N et al.Cancer genetics and cytogenetics. 1998, Vol 104, Num 2, pp 133-138, issn 0165-4608Article