UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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

Volltextzugriff (PDF)

Classification Of Forested Terrain Using Multifrequency, Polarimetric Sap, Data

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

1990

Volltextzugriff (PDF)

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

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)

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

Volltextzugriff (PDF)

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

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

1999

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

1992

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

1990

Volltextzugriff (PDF)

Monosomy 8p: an easily overlooked syndrome

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

1986

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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)

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

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)

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

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

1993

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

1992

Volltextzugriff (PDF)

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

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

1992

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Trisomy 13 and myelodysplastic syndrome

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

1990

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Aktive Filter

KollektionWiley Online Library Full Collection 2018

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(18)
Mit Volltextzugriff
(18)

Publikationsform

Sprache

Englisch
(28)
Niederländisch
(1)

Erscheinungsjahr

n.n

Thema

Biological And Medical Sciences
(21)
Humans
(20)
Medical Sciences
(20)
Life Sciences & Biomedicine
(19)
Science & Technology
(19)
Hematologic And Hematopoietic Diseases
(14)
Leukemias. Malignant Lymphomas. Malignant Reticulosis. Myelofibrosis
(13)
Male
(12)
Genetics & Heredity
(10)
Oncology
(9)
Adult
(8)
Female
(8)
Karyotyping
(7)
Chromosome Aberrations
(6)
Middle Aged
(6)
Translocation, Genetic
(6)
Chromosomes, Human, Pair 14
(5)
Chromosomes, Human, Pair 8
(5)
Hematology
(5)
Aged
(4)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

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

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

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

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

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

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

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

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

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

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

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

Aktive Filter

Suchergebnisse filtern