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LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia

Genes chromosomes & cancer, 2002-09, Vol.35 (1), p.92-96

2002

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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

1988

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Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment

Prenatal diagnosis, 1998-10, Vol.18 (10), p.1082-1085

1998

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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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A novel t(6;14)(q25∼q27;q32) in acute myelocytic leukemia involves the BCL11B gene

Cancer genetics and cytogenetics, 2004-02, Vol.149 (1), p.72-76

2004

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Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3

American journal of human genetics, 1993-02, Vol.52 (2), p.249-254

1993

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Proliferation and Cytogenetic Analysis of Hairy Cell Leukemia Upon Stimulation Via the CD40 Antigen

Blood, 1994-11, Vol.84 (9), p.3134-3141

1994

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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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Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3

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

1997

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Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis: A Case Report and Review of the Literature

Cancer genetics and cytogenetics, 1999-11, Vol.115 (1), p.11-18

1999

Volltextzugriff (PDF)

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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Premature menopause because of an inherited deletion in the long arm of the X-chromosome

Fertility and sterility, 1991-03, Vol.55 (3), p.631-633

1991

Volltextzugriff (PDF)

Somatic pairing of centromeres and short arms of chromosome 15 in the hematopoietic and lymphoid system

Human genetics, 1993-12, Vol.92 (6), p.577-582

1993

Volltextzugriff (PDF)

Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree

Genes chromosomes & cancer, 1995-07, Vol.13 (3), p.192-202

1995

Volltextzugriff (PDF)

LETTER TO THE EDITOR. YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME 18 HETERMORPHISMS?

Prenatal diagnosis, 1997-06, Vol.17 (6), p.585-586

1997

Volltextzugriff (PDF)

Sequential development of peripheral T‐cell lymphoma in the course of chronic myelogenous leukemia

Cancer, 1990-09, Vol.66 (6), p.1198-1203

1990

Volltextzugriff (PDF)

Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies

Genes chromosomes & cancer, 1992-03, Vol.4 (2), p.128-134

1992

Volltextzugriff (PDF)

Haematopoietic and immunologic abnormalities in severe aplastic anaemia patients treated with anti‐thymocyte globulin

British journal of haematology, 1989-03, Vol.71 (3), p.421-430

1989

Volltextzugriff (PDF)

Fetal blood group determination in first-trimester pregnancy for the management of severe immunization

American journal of obstetrics and gynecology, 1987-01, Vol.156 (1), p.120-123

1987

Volltextzugriff (PDF)

T‐cell prolymphocytic leukemia with an unusual phenotype CD4+ CD8

Cancer, 1987-08, Vol.60 (4), p.794-803

1987

Volltextzugriff (PDF)

Characterization of a New Human B Cell Line (Bonna-12) with Trisomy 9 and Trisomy 12 Chromosomal Abnormality

Leukemia & lymphoma, 1991, Vol.5 (5-6), p.415-422

1991

Volltextzugriff (PDF)

Fetal cell detection in maternal blood: A study in 236 samples using erythroblast morphology, DAB and Hbf staining, and FISH analysis

Cytometry (New York, N.Y.), 1998-07, Vol.32 (3), p.178-185

1998

Volltextzugriff (PDF)

Development of a preparation and staining method for fetal erythroblasts in maternal blood: Simultaneous immunocytochemical staining and FISH analysis

Cytometry (New York, N.Y.), 1998-07, Vol.32 (3), p.170-177

1998

Volltextzugriff (PDF)

A second case of hexasomy 8 in myelodysplastic syndrome

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

1997

Volltextzugriff (PDF)

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LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia

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

Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment

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

A novel t(6;14)(q25∼q27;q32) in acute myelocytic leukemia involves the BCL11B gene

Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3

Proliferation and Cytogenetic Analysis of Hairy Cell Leukemia Upon Stimulation Via the CD40 Antigen

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

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

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3

Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis: A Case Report and Review of the Literature

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

Premature menopause because of an inherited deletion in the long arm of the X-chromosome

Somatic pairing of centromeres and short arms of chromosome 15 in the hematopoietic and lymphoid system

Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree

LETTER TO THE EDITOR. YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME 18 HETERMORPHISMS?

Sequential development of peripheral T‐cell lymphoma in the course of chronic myelogenous leukemia

Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies

Haematopoietic and immunologic abnormalities in severe aplastic anaemia patients treated with anti‐thymocyte globulin

Fetal blood group determination in first-trimester pregnancy for the management of severe immunization

T‐cell prolymphocytic leukemia with an unusual phenotype CD4+ CD8

Characterization of a New Human B Cell Line (Bonna-12) with Trisomy 9 and Trisomy 12 Chromosomal Abnormality

Fetal cell detection in maternal blood: A study in 236 samples using erythroblast morphology, DAB and Hbf staining, and FISH analysis

Development of a preparation and staining method for fetal erythroblasts in maternal blood: Simultaneous immunocytochemical staining and FISH analysis

A second case of hexasomy 8 in myelodysplastic syndrome

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