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...

A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

Human genetics, 2004-03, Vol.114 (4), p.349-353

2004

Volltextzugriff (PDF)

A Major Predisposition Locus for Severe Obesity, at 4p15-p14

American journal of human genetics, 2002-06, Vol.70 (6), p.1459-1468

2002

Volltextzugriff (PDF)

Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred

Arteriosclerosis, thrombosis, and vascular biology, 2000-04, Vol.20 (4), p.1089-1093

2000

Volltextzugriff (PDF)

Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

Science (American Association for the Advancement of Science), 1990-06, Vol.248 (4960), p.1224-1227

1990

Volltextzugriff (PDF)

TBC1D1 is a candidate for a severe obesity gene and evidence for a gene/gene interaction in obesity predisposition

Human molecular genetics, 2006-09, Vol.15 (18), p.2709-2720

2006

Volltextzugriff (PDF)

Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-05, Vol.135B (1), p.85-93

2005

Volltextzugriff (PDF)

Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

The New England journal of medicine, 1988-09, Vol.319 (9), p.533-537

1988

Volltextzugriff (PDF)

Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series

Journal of human genetics, 2002-01, Vol.47 (12), p.641-648

2002

Volltextzugriff (PDF)

Prevalence of hemochromatosis among 11,065 presumably healthy blood donors

The New England journal of medicine, 1988-05, Vol.318 (21), p.1355-1362

1988

Volltextzugriff (PDF)

Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM)

Cancer research (Chicago, Ill.), 1994-12, Vol.54 (23), p.6041-6044

1994

Volltextzugriff (PDF)

Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2

American journal of human genetics, 2003-12, Vol.73 (6), p.1271-1281

2003

Volltextzugriff (PDF)

Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor

Cancer research (Chicago, Ill.), 1997-10, Vol.57 (19), p.4177-4182

1997

Volltextzugriff (PDF)

Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

American journal of clinical pathology, 1982-08, Vol.78 (2), p.196-207

1982

Volltextzugriff (PDF)

A probabilistic model for detecting coding regions in DNA sequences

Mathematical medicine and biology, 1994, Vol.11 (3), p.149-160

1994

Volltextzugriff (PDF)

Global fractal dimension of human DNA sequences treated as pseudorandom walks

Physical review. A, Atomic, molecular, and optical physics, 1992-06, Vol.45 (12), p.8902-8913

1992

Volltextzugriff (PDF)

Interobserver concordance in discriminating clinical atypia of melanocytic nevi, and correlations with histologic atypia

Journal of the American Academy of Dermatology, 1996-04, Vol.34 (4), p.618-625

1996

Volltextzugriff (PDF)

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

Oncogene, 1996-10, Vol.13 (7), p.1483-1488

1996

Volltextzugriff (PDF)

Familial Associations between Cancer Sites

Computers and biomedical research, 1999-12, Vol.32 (6), p.517-529

1999

Volltextzugriff (PDF)

A multiobserver, population-based analysis of histologic dysplasia in melanocytic nevi

Journal of the American Academy of Dermatology, 1994-05, Vol.30 (5), p.707-714

1994

Volltextzugriff (PDF)

Prevalence of hemochromatosis

The New England journal of medicine, 1988-12, Vol.319 (23), p.1548-1549

1988

Volltextzugriff (PDF)

Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

The New England journal of medicine, 1989-02, Vol.320 (5), p.316-317

1989

Volltextzugriff (PDF)

The future of DNA diagnostics

Disease markers, 1999-10, Vol.15 (1-3), p.106-107

SKOLNICK, M. H

1999

Volltextzugriff (PDF)

Mutations in the BRCA1 gene in Japanese breast cancer patients

Human mutation, 1996, Vol.7 (4), p.334-339

1996

Volltextzugriff (PDF)

The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype

Journal of the American Academy of Dermatology, 1989-03, Vol.20 (3), p.407-415

1989

Volltextzugriff (PDF)

1 – 25 von 81

Suche als RSS-Feed

Aktive Filter

ThemaTumors

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(70)
Mit Volltextzugriff
(66)

Publikationsform

Sprache

Englisch
(81)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

A Major Predisposition Locus for Severe Obesity, at 4p15-p14

Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred

Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

TBC1D1 is a candidate for a severe obesity gene and evidence for a gene/gene interaction in obesity predisposition

Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders

Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

Association of common missense changes in ELAC2 ( HPC2) with prostate cancer in a Japanese case-control series

Prevalence of hemochromatosis among 11,065 presumably healthy blood donors

Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM)

A candidate prostate cancer susceptibility gene at chromosome 17p

Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2

Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor

Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

A probabilistic model for detecting coding regions in DNA sequences

Global fractal dimension of human DNA sequences treated as pseudorandom walks

Interobserver concordance in discriminating clinical atypia of melanocytic nevi, and correlations with histologic atypia

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations

Familial Associations between Cancer Sites

A multiobserver, population-based analysis of histologic dysplasia in melanocytic nevi

Prevalence of hemochromatosis

Common inheritance of susceptibility to colonic adenomatous polyps and associated colorectal cancers

The future of DNA diagnostics

Mutations in the BRCA1 gene in Japanese breast cancer patients

The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype

Aktive Filter

Suchergebnisse filtern