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...

Quantitation of Aurora Kinase A Gene Copy Number in Urine Sediments and Bladder Cancer Detection

JNCI : Journal of the National Cancer Institute, 2008-10, Vol.100 (19), p.1401-1411

2008

Volltextzugriff (PDF)

Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

Archives of pathology & laboratory medicine (1976), 2010-07, Vol.134 (7), p.1010-1015

2010

Volltextzugriff (PDF)

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

Genetics in Medicine Open, 2024, Vol.2, p.101820, Article 101820

2024

Volltextzugriff (PDF)

A Pharmacogenetic versus a Clinical Algorithm for Warfarin Dosing

The New England journal of medicine, 2013-12, Vol.369 (24), p.2283-2293

2013

Volltextzugriff (PDF)

Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia

Pediatric Blood & Cancer, 2008-08, Vol.51 (2), p.171-177

2008

Volltextzugriff (PDF)

Deletion of the Short Arm of Chromosome 1 (del 1p) is a Strong Predictor of Poor Outcome in Myeloma Patients Undergoing an Autotransplant

Biology of blood and marrow transplantation, 2007-09, Vol.13 (9), p.1066-1072

2007

Volltextzugriff (PDF)

Identification of the Novel Chromosomal Translocation t(17;19)(q23;q13) in a Pediatric Patient with Acute Myeloid Leukemia

Blood, 2005-11, Vol.106 (11), p.4344-4344

2005

Volltextzugriff (PDF)

Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

Archives of pathology & laboratory medicine (1976), 2010-07, Vol.134 (7), p.1010-1015

2010

Volltextzugriff (PDF)

Melodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

Archives of pathology & laboratory medicine (1976), 2010-07, Vol.134 (7), p.1010

2010

Volltextzugriff (PDF)

C/EBPβ suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL

Cancer genetics and cytogenetics, 2007-09, Vol.177 (2), p.108-114

2007

Volltextzugriff (PDF)

C/EBPbeta suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL

Cancer genetics and cytogenetics, 2007-09, Vol.177 (2), p.108-114

2007

Volltextzugriff (PDF)

Stromal Fibroblasts Present in Invasive Human Breast Carcinomas Promote Tumor Growth and Angiogenesis through Elevated SDF-1/CXCL12 Secretion

Cell, 2005-05, Vol.121 (3), p.335-348

2005

Volltextzugriff (PDF)

Overexpression of Eg5 Causes Genomic Instability and Tumor Formation in Mice

Cancer research (Chicago, Ill.), 2007-11, Vol.67 (21), p.10138-10147

2007

Volltextzugriff (PDF)

Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain

Cancer research (Chicago, Ill.), 2004-08, Vol.64 (15), p.5140-5147

2004

Volltextzugriff (PDF)

A patient with isochromosome 18q, radial‐thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation

American journal of medical genetics, 2005-02, Vol.133A (1), p.93-98

2005

Volltextzugriff (PDF)

Tyrosine kinase activation in breast carcinoma with correlation to HER-2/neu gene amplification and receptor overexpression

Human pathology, 2001-12, Vol.32 (12), p.1344-1350

2001

Volltextzugriff (PDF)

Loss of Heterozygosity Occurs via Mitotic Recombination in Trp53 super(+/-) Mice and Associates with Mammary Tumor Susceptibility of the BALB/c Strain

Cancer research (Chicago, Ill.), 2004-08, Vol.64 (15), p.5140-5147

2004

Volltextzugriff (PDF)

Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism

Journal of perinatology, 1998-09, Vol.18 (5), p.395-398

1998

Volltextzugriff (PDF)

De novo translocation (8;12) and frontofacionasal dysplasia in a newborn boy

American journal of medical genetics, 2000-09, Vol.94 (3), p.179-183

2000

Volltextzugriff (PDF)

1 – 20 von 20

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(16)
Mit Volltextzugriff
(19)

Publikationsform

Artikel
(20)

Sprache

Englisch
(20)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(12)
Science & Technology
(12)
Humans
(11)
Female
(9)
Male
(8)
Biological And Medical Sciences
(7)
Karyotyping
(7)
Medical Sciences
(7)
In Situ Hybridization, Fluorescence
(5)
Oncology
(5)
Tumors
(5)
Adult
(4)
Infant
(4)
Aged
(3)
Animals
(3)
Child
(3)
Chromosome Aberrations
(3)
Follow-Up Studies
(3)
Genetics & Heredity
(3)
Hematology, Oncology And Palliative Medicine
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Quantitation of Aurora Kinase A Gene Copy Number in Urine Sediments and Bladder Cancer Detection

Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

A Pharmacogenetic versus a Clinical Algorithm for Warfarin Dosing

Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia

Atlas of Cytogenomics in Oncology and Hematology: a Platform-Neutral Clinical Cancer Genomics Database

Deletion of the Short Arm of Chromosome 1 (del 1p) is a Strong Predictor of Poor Outcome in Myeloma Patients Undergoing an Autotransplant

Identification of the Novel Chromosomal Translocation t(17;19)(q23;q13) in a Pediatric Patient with Acute Myeloid Leukemia

Myelodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

Melodysplastic syndromes arising in patients with germline TP53 mutation and Li-Fraumeni syndrome

C/EBPβ suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL

C/EBPbeta suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL

Stromal Fibroblasts Present in Invasive Human Breast Carcinomas Promote Tumor Growth and Angiogenesis through Elevated SDF-1/CXCL12 Secretion

Overexpression of Eg5 Causes Genomic Instability and Tumor Formation in Mice

Loss of heterozygosity occurs via mitotic recombination in Trp53+/- mice and associates with mammary tumor susceptibility of the BALB/c strain

A patient with isochromosome 18q, radial‐thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation

Tyrosine kinase activation in breast carcinoma with correlation to HER-2/neu gene amplification and receptor overexpression

Loss of Heterozygosity Occurs via Mitotic Recombination in Trp53 super(+/-) Mice and Associates with Mammary Tumor Susceptibility of the BALB/c Strain

Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism

De novo translocation (8;12) and frontofacionasal dysplasia in a newborn boy

Suchergebnisse filtern