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Activation of the c-myc oncogene in a precursor-B-cell blast crisis of follicular lymphoma, presenting as composite lymphoma

The New England journal of medicine, 1988-05, Vol.318 (21), p.1373-1378

1988

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A new non-Hodgkin's B-cell line (DoHH2) with a chromosomal translocation t(14;18) (q32,q21)

Leukemia, 1991-03, Vol.5 (3), p.221-224

1991

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RT-PCR Diagnosis of Patients With Acute Nonlymphocytic Leukemia and inv(16)(pl3q22) and Identification of New Alternative Splicing in CBFB-MYH11 Transcripts

Blood, 1995-07, Vol.86 (1), p.277-282

1995

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Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults

British journal of haematology, 1988-09, Vol.70 (1), p.55-62

1988

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Effect of subcutaneously administered human recombinant erythropoietin on erythropoiesis in patients with myelodysplasia

British journal of haematology, 1991-08, Vol.78 (4), p.488-493

1991

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Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells

Blood, 1992-08, Vol.80 (3), p.750-757

1992

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PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

Prenatal diagnosis, 1997-02, Vol.17 (2), p.173-179

1997

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De novo acute B-cell leukemia with translocation t(14;18) : an entity with a poor prognosis

Leukemia, 1991-06, Vol.5 (6), p.473-478

1991

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46,XY del(18) (q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome

Clinical genetics, 1993-02, Vol.43 (2), p.76-78

1993

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Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male

Journal of medical genetics, 1989-05, Vol.26 (5), p.330-333

1989

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Chromosome abnormalities in a patient with acquired immunodeficiency syndrome (AIDS) and Burkitt lymphoma-leukemia

Leukemia, 1990-06, Vol.4 (6), p.445-447

1990

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A patient with an interstitial deletion of the short arm of chromosome 6

Clinical genetics, 1988-02, Vol.33 (2), p.95-101

1988

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Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3

Journal of medical genetics, 1997-07, Vol.34 (7), p.569-572

1997

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The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986

Clinical genetics, 1988-06, Vol.33 (6), p.410-417

1988

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t(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia

Cancer genetics and cytogenetics, 1993, Vol.65 (1), p.7-11

1993

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A second case of hexasomy 8 in myelodysplastic syndrome

Cancer genetics and cytogenetics, 1997-11, Vol.99 (1), p.68-72

1997

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Trisomy 13 and myelodysplastic syndrome

Cancer genetics and cytogenetics, 1990-09, Vol.48 (2), p.179-182

1990

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Chimerism pattern following allogeneic bone marrow transplantation; a retrospective study of the connection with post-transplantation complications

Nederlands tijdschrift voor geneeskunde, 1990-05, Vol.134 (18), p.908

1990

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Activation of the c-myc oncogene in a precursor-B-cell blast crisis of follicular lymphoma, presenting as composite lymphoma

A new non-Hodgkin's B-cell line (DoHH2) with a chromosomal translocation t(14;18) (q32,q21)

RT-PCR Diagnosis of Patients With Acute Nonlymphocytic Leukemia and inv(16)(pl3q22) and Identification of New Alternative Splicing in CBFB-MYH11 Transcripts

Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults

Effect of subcutaneously administered human recombinant erythropoietin on erythropoiesis in patients with myelodysplasia

Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

De novo acute B-cell leukemia with translocation t(14;18) : an entity with a poor prognosis

46,XY del(18) (q21.3q22.2) with mosaicism of r(18) and a milder form of the 18q- syndrome

Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male

Chromosome abnormalities in a patient with acquired immunodeficiency syndrome (AIDS) and Burkitt lymphoma-leukemia

A patient with an interstitial deletion of the short arm of chromosome 6

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3

The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986

t(5;12)(q31;p12) A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia

A second case of hexasomy 8 in myelodysplastic syndrome

Trisomy 13 and myelodysplastic syndrome

Chimerism pattern following allogeneic bone marrow transplantation; a retrospective study of the connection with post-transplantation complications

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