UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 615

Sortiert nach

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Nature genetics, 2017-02, Vol.49 (2), p.223-237

2017

Link zum Volltext

Verfügbarkeit prüfen

Tumor protein D52 (TPD52) is overexpressed and a gene amplification target in ovarian cancer

International journal of cancer, 2005-12, Vol.117 (6), p.1049-1054

2005

Link zum Volltext

Verfügbarkeit prüfen

Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant

Human mutation, 2018-03, Vol.39 (3), p.383-388

2018

Link zum Volltext

Verfügbarkeit prüfen

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

European journal of human genetics : EJHG, 2013-05, Vol.21 (5), p.522-527

2013

Link zum Volltext

Verfügbarkeit prüfen

A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings

American journal of medical genetics. Part A, 2016-07, Vol.170A (7), p.1930-1933

2016

Link zum Volltext

Verfügbarkeit prüfen

Gender Modification and Resource Allocation in Subdioecious Wurmbea dioica (Colchicaceae)

The Journal of ecology, 1999-02, Vol.87 (1), p.123-137

1999

Link zum Volltext

Verfügbarkeit prüfen

Challenges in identifying candidate amplification targets in human cancers: chromosome 8q21 as a case study

Genes & cancer, 2012-02, Vol.3 (2), p.87-101

2012

Link zum Volltext

Verfügbarkeit prüfen

Challenges in Identifying Candidate Amplification Targets in Human Cancers: Chromosome 8q21 as a Case Study

Genes & cancer, 2012-02, Vol.3 (2), p.87-101

2012

Link zum Volltext

Verfügbarkeit prüfen

Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome

American journal of medical genetics, 2005-02, Vol.132A (4), p.381-385

2005

Link zum Volltext

Verfügbarkeit prüfen

Concurrent transposition of distal 6p and 20q to the 22q telomere: A recurrent benign chromosomal variant

European journal of medical genetics, 2008-03, Vol.51 (2), p.148-155

2008

Link zum Volltext

Verfügbarkeit prüfen

Nemaline myopathy and distal arthrogryposis associated with an autosomal recessiveￂ TNNT3ￂ splice variant

Human mutation, 2018-03, Vol.39 (3), p.383

2018

Link zum Volltext

Verfügbarkeit prüfen

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Nature genetics, 2017-06, Vol.49 (6), p.969-969

2017

Link zum Volltext

Verfügbarkeit prüfen

Erratum: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Nature genetics, 2017-06, Vol.49 (6), p.969-969

2017

Link zum Volltext

Verfügbarkeit prüfen

The (4;11)(q21;p15) translocation fuses the NUP98 and RAP1GDS1 genes and is recurrent in T-cell acute lymphocytic leukemia

Blood, 1999-09, Vol.94 (6), p.2072-2079

1999

Link zum Volltext

Verfügbarkeit prüfen

The (4;11)(q21;p15) Translocation Fuses the NUP98 andRAP1GDS1 Genes and Is Recurrent in T-Cell Acute Lymphocytic Leukemia

Blood, 1999-09, Vol.94 (6), p.2072-2079

1999

Link zum Volltext

Verfügbarkeit prüfen

The (4;11)(q21;p15) Translocation Fuses the NUP98 andRAP1GDS1 Genes and Is Recurrent in T-Cell Acute Lymphocytic Leukemia

Blood, 1999-09, Vol.94 (6), p.2072-2079

1999

Link zum Volltext

Verfügbarkeit prüfen

Localization of the human growth arrest-specific gene (GAS1) to chromosome bands 9q21.3-q22, a region frequently deleted in myeloid malignancies

Genomics (San Diego, Calif.), 1993-12, Vol.18 (3), p.731-733

1993

Link zum Volltext

Verfügbarkeit prüfen

A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings

American journal of medical genetics. Part A, 2016, Vol.170 (7), p.1930-1933

2016

Link zum Volltext

Verfügbarkeit prüfen

Mapping of the chromosome 11 breakpoint of the t(4;11)(q21;p14–15) translocation

Cancer genetics and cytogenetics, 1993-09, Vol.69 (2), p.122-125

1993

Link zum Volltext

Verfügbarkeit prüfen

Novel translocations in acute nonlymphocytic leukemia

Cancer genetics and cytogenetics, 1990-01, Vol.44 (1), p.99-105

1990

Link zum Volltext

Verfügbarkeit prüfen

Novel translocations in acute nonlymphocytic leukemia: Two cases involving chromosome 21, band q22

Cancer genetics and cytogenetics, 1990, Vol.44 (1), p.99-105

1990

Link zum Volltext

Verfügbarkeit prüfen

A rare translocation (4;11)(q21;p14–15) in an acute lymphoblastic leukemia expressing T-cell and myeloid markers

Cancer genetics and cytogenetics, 1991-10, Vol.56 (2), p.255-262

1991

Link zum Volltext

Verfügbarkeit prüfen

Ultra-efficient frequency comb generation in AlGaAs-on-insulator microresonators

Nature communications, 2020-03, Vol.11 (1), p.1331-1331, Article 1331

2020

Link zum Volltext

Verfügbarkeit prüfen

Seasonal distribution and historic trends in abundance of white sharks, Carcharodon carcharias, in the western North Atlantic Ocean

PloS one, 2014-06, Vol.9 (6), p.e99240-e99240

2014

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 615

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(573)
Mit Volltextzugriff
(515)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(615)
Japanisch
(108)
Norwegisch
(5)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(10)

Menü

Weitere Dienste

Einstellungen

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Tumor protein D52 (TPD52) is overexpressed and a gene amplification target in ovarian cancer

Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings

Gender Modification and Resource Allocation in Subdioecious Wurmbea dioica (Colchicaceae)

Challenges in identifying candidate amplification targets in human cancers: chromosome 8q21 as a case study

Challenges in Identifying Candidate Amplification Targets in Human Cancers: Chromosome 8q21 as a Case Study

Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome

Concurrent transposition of distal 6p and 20q to the 22q telomere: A recurrent benign chromosomal variant

Nemaline myopathy and distal arthrogryposis associated with an autosomal recessiveￂ TNNT3ￂ splice variant

Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

Erratum: Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

The (4;11)(q21;p15) translocation fuses the NUP98 and RAP1GDS1 genes and is recurrent in T-cell acute lymphocytic leukemia

The (4;11)(q21;p15) Translocation Fuses the NUP98 andRAP1GDS1 Genes and Is Recurrent in T-Cell Acute Lymphocytic Leukemia

The (4;11)(q21;p15) Translocation Fuses the NUP98 andRAP1GDS1 Genes and Is Recurrent in T-Cell Acute Lymphocytic Leukemia

Localization of the human growth arrest-specific gene (GAS1) to chromosome bands 9q21.3-q22, a region frequently deleted in myeloid malignancies

A balanced paternal interchromosomal reciprocal insertion between 5q12.1q13.2 and 20p12.3p12.1 resulting in separate genetic conditions in two siblings

Mapping of the chromosome 11 breakpoint of the t(4;11)(q21;p14–15) translocation

Novel translocations in acute nonlymphocytic leukemia

Novel translocations in acute nonlymphocytic leukemia: Two cases involving chromosome 21, band q22

A rare translocation (4;11)(q21;p14–15) in an acute lymphoblastic leukemia expressing T-cell and myeloid markers

Ultra-efficient frequency comb generation in AlGaAs-on-insulator microresonators

Seasonal distribution and historic trends in abundance of white sharks, Carcharodon carcharias, in the western North Atlantic Ocean

Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype

Suchergebnisse filtern