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Establishment and characterization of an uveal‐melanoma cell line

International journal of cancer, 1995-07, Vol.62 (2), p.155-161

1995

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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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Amniocentesis before 14 completed weeks as an alternative to transabdominal chorionic villus sampling: a controlled trial with infant follow-up

Prenatal diagnosis, 1998-05, Vol.18 (5), p.465-475

1998

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Monosomy 8p: an easily overlooked syndrome

Journal of medical genetics, 1986-04, Vol.23 (2), p.153-154

1986

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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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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

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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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Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome

Clinical genetics, 1984-07, Vol.26 (1), p.65-68

1984

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A girl with 71,XXXXY karyotype

Clinical genetics, 1992-02, Vol.41 (2), p.96-99

1992

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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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A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia

Cancer genetics and cytogenetics, 1996-07, Vol.89 (2), p.132-135

1996

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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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Establishment and characterization of an uveal‐melanoma cell line

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

Amniocentesis before 14 completed weeks as an alternative to transabdominal chorionic villus sampling: a controlled trial with infant follow-up

Monosomy 8p: an easily overlooked syndrome

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

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

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

Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome

A girl with 71,XXXXY karyotype

A second case of hexasomy 8 in myelodysplastic syndrome

A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia

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

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