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...

The Fine-Scale Structure of Recombination Rate Variation in the Human Genome

Science (American Association for the Advancement of Science), 2004-04, Vol.304 (5670), p.581-584

2004

Volltextzugriff (PDF)

A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms

American journal of human genetics, 2005-04, Vol.76 (4), p.634-646

2005

Volltextzugriff (PDF)

A comprehensive catalogue of somatic mutations from a human cancer genome

Nature (London), 2010-01, Vol.463 (7278), p.191-196

2010

Volltextzugriff (PDF)

Analysis of vertebrate SCL loci identifies conserved enhancers

Nature biotechnology, 2000-02, Vol.18 (2), p.181-186

2000

Volltextzugriff (PDF)

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

Nature (London), 1993-01, Vol.361 (6409), p.226-233

1993

Volltextzugriff (PDF)

Chromosome 20 deletions in myeloid malignancies : reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

Oncogene, 2000-08, Vol.19 (34), p.3902-3913

2000

Volltextzugriff (PDF)

A first-generation linkage disequilibrium map of human chromosome 22

Nature (London), 2002-08, Vol.418 (6897), p.544-548

2002

Volltextzugriff (PDF)

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

Nature genetics, 1998-10, Vol.20 (2), p.129-135

1998

Volltextzugriff (PDF)

Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach

Pharmacogenetics and genomics, 2007-03, Vol.17 (3), p.217-220

2007

Volltextzugriff (PDF)

Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)

Epilepsy research, 2011-09, Vol.96 (1), p.109-115

2011

Volltextzugriff (PDF)

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples

Human molecular genetics, 2004-11, Vol.13 (21), p.2557-2565

2004

Volltextzugriff (PDF)

A comparison of tagging methods and their tagging space

Human molecular genetics, 2005-09, Vol.14 (18), p.2757-2767

2005

Volltextzugriff (PDF)

Mapping copy number variation by population-scale genome sequencing

Nature (London), 2011-02, Vol.470 (7332), p.59-65

2011

Volltextzugriff (PDF)

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

Nature (London), 1984, Vol.307 (5948), p.237-241

1984

Volltextzugriff (PDF)

Diversity of Human Copy Number Variation and Multicopy Genes

Science (American Association for the Advancement of Science), 2010-10, Vol.330 (6004), p.641-646

2010

Volltextzugriff (PDF)

Variation in genome-wide mutation rates within and between human families

Nature genetics, 2011-07, Vol.43 (7), p.712-714

2011

Volltextzugriff (PDF)

A second generation human haplotype map of over 3.1 million SNPs

Nature, 2007-10, Vol.449 (7164), p.851-861

2007

Volltextzugriff (PDF)

Point Mutations in the Dystrophin Gene

Proceedings of the National Academy of Sciences - PNAS, 1992-03, Vol.89 (6), p.2331-2335

1992

Volltextzugriff (PDF)

Genome-wide detection and characterization of positive selection in human populations

Nature, 2007-10, Vol.449 (7164), p.913-918

2007

Volltextzugriff (PDF)

Exon Structure of the Human Dystrophin Gene

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.536-538

1993

Volltextzugriff (PDF)

A physical map of the mouse genome

Nature (London), 2002-08, Vol.418 (6899), p.743-750

2002

Volltextzugriff (PDF)

Integrating ethics and science in the International HapMap Project

Nature reviews. Genetics, 2004-06, Vol.5 (6), p.467-475

Foster, Morris W

2004

Volltextzugriff (PDF)

A 6.9-Mb High-Resolution BAC/PAC Contig of Human 4p15.3–p16.1, a Candidate Region for Bipolar Affective Disorder

Genomics (San Diego, Calif.), 2001-02, Vol.71 (3), p.315-323

2001

Volltextzugriff (PDF)

Detection of point mutations and a gross deletion in six Hunter Syndrome patients

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.543-550

1992

Volltextzugriff (PDF)

1 – 25 von 136

Suche als RSS-Feed

Aktive Filter

ThemaBiological And Medical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(133)
Mit Volltextzugriff
(128)

Publikationsform

Artikel
(136)

Sprache

Englisch
(136)
Japanisch
(38)

Erscheinungsjahr

n.n

Thema

Science & Technology
(117)
Life Sciences & Biomedicine
(101)
Humans
(94)
Medical Sciences
(73)
Fundamental And Applied Biological Sciences. Psychology
(71)
Female
(49)
Male
(44)
Genetics & Heredity
(29)
Adult
(27)
Animals
(25)
Molecular Sequence Data
(23)
Molecular And Cellular Biology
(22)
Genes
(21)
Biotechnology & Applied Microbiology
(19)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(19)
Base Sequence
(17)
Human
(17)
Middle Aged
(17)
Pharmacology. Drug Treatments
(17)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The Fine-Scale Structure of Recombination Rate Variation in the Human Genome

A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms

A comprehensive catalogue of somatic mutations from a human cancer genome

Analysis of vertebrate SCL loci identifies conserved enhancers

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

Chromosome 20 deletions in myeloid malignancies : reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes

A first-generation linkage disequilibrium map of human chromosome 22

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

Identification of the breast cancer susceptibility gene BRCA2

Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach

Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples

A comparison of tagging methods and their tagging space

Mapping copy number variation by population-scale genome sequencing

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

Diversity of Human Copy Number Variation and Multicopy Genes

Variation in genome-wide mutation rates within and between human families

A second generation human haplotype map of over 3.1 million SNPs

Point Mutations in the Dystrophin Gene

Genome-wide detection and characterization of positive selection in human populations

Exon Structure of the Human Dystrophin Gene

A physical map of the mouse genome

Integrating ethics and science in the International HapMap Project

A 6.9-Mb High-Resolution BAC/PAC Contig of Human 4p15.3–p16.1, a Candidate Region for Bipolar Affective Disorder

Detection of point mutations and a gross deletion in six Hunter Syndrome patients

Aktive Filter

Suchergebnisse filtern