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Estimation of 3-D Ocean Wave Spectra from Spotlight Sar Data During Saxon-Fpn

[Proceedings] IGARSS '92 International Geoscience and Remote Sensing Symposium, 1992, Vol.2, p.1097-1099

1992

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Classification Of Forested Terrain Using Multifrequency, Polarimetric Sap, Data

10th Annual International Symposium on Geoscience and Remote Sensing, 1990, p.2401-2401

1990

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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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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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Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature

American journal of medical genetics, 2003-10, Vol.122A (2), p.168-173

2003

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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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Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

Oncogene, 1999-01, Vol.18 (2), p.543-550

1999

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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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Translocation t(14;18) in B cell lymphomas as a cause for defective immunoglobulin production

The Journal of experimental medicine, 1989-03, Vol.169 (3), p.613-624

1989

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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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Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia

Leukemia, 1996-09, Vol.10 (9), p.1459-1462

1996

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Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

Cytogenetic and genome research, 1990-01, Vol.53 (2-3), p.126-128

1990

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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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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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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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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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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

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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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Estimation of 3-D Ocean Wave Spectra from Spotlight Sar Data During Saxon-Fpn

Classification Of Forested Terrain Using Multifrequency, Polarimetric Sap, Data

Establishment and characterization of an uveal‐melanoma cell line

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

Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature

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

Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

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

Translocation t(14;18) in B cell lymphomas as a cause for defective immunoglobulin production

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

Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p

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

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

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

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

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

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

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