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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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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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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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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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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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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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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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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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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 FLUORESCENCEIN SITU HYBRIDIZATION

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

1997

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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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The Evolution of Species of the Varanidae - Microcomplement Fixation Analysis of Serum Albumins

Australian journal of zoology, 1993, Vol.41 (6), p.621

1993

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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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Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemia precursor cells

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

1992

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Combined immunoophenotyping and DNA in situ hybridization to study ineage involvement in patients with myelodysplatic syndromes

Blood, 1992, Vol.79 (7), p.1823-1828

1992

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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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Update of the cytogenetic study of childhood non-high-risk acute lymphocytic leukemia at diagnosis in protocol VI of the Dutch Childhood Leukemia Study Group

Haematology and blood transfusion, 1990, Vol.33, p.169

1990

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Electronics in New Zealand

Superintendent of Documents, March 1947. 4 pp, 1947

1947

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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

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)

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

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

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

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

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

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

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 FLUORESCENCEIN SITU HYBRIDIZATION

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

The Evolution of Species of the Varanidae - Microcomplement Fixation Analysis of Serum Albumins

Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemic precursor cells

Effect of mast cell growth factor (c-kit ligand) on clonogenic leukemia precursor cells

Combined immunoophenotyping and DNA in situ hybridization to study ineage involvement in patients with myelodysplatic syndromes

Trisomy 13 and myelodysplastic syndrome

Update of the cytogenetic study of childhood non-high-risk acute lymphocytic leukemia at diagnosis in protocol VI of the Dutch Childhood Leukemia Study Group

Electronics in New Zealand

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