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...

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

Human genetics, 2009-04, Vol.125 (3), p.257-263

2009

Volltextzugriff (PDF)

The impact of race as a risk factor for symptom severity and age at diagnosis of uterine leiomyomata among affected sisters

American journal of obstetrics and gynecology, 2008-02, Vol.198 (2), p.168.e1-168.e9

2008

Volltextzugriff (PDF)

MDR1 Ala893 Polymorphism Is Associated with Inflammatory Bowel Disease

American journal of human genetics, 2003-12, Vol.73 (6), p.1282-1292

2003

Volltextzugriff (PDF)

Polymorphisms in the Insulin-Degrading Enzyme Gene Are Associated With Type 2 Diabetes in Men From the NHLBI Framingham Heart Study

Diabetes (New York, N.Y.), 2003-06, Vol.52 (6), p.1562-1567

2003

Volltextzugriff (PDF)

Involvement of fumarate hydratase in nonsyndromic uterine leiomyomas: Genetic linkage analysis and FISH studies

Genes chromosomes & cancer, 2004-11, Vol.41 (3), p.183-190

2004

Volltextzugriff (PDF)

Variation and heritability of Hb F and F‐cells among β‐thalassemia heterozygotes in Hong Kong

American journal of hematology, 2008-06, Vol.83 (6), p.458-464

2008

Volltextzugriff (PDF)

Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis

Human molecular genetics, 2004-01, Vol.13 (1), p.35-45

2004

Volltextzugriff (PDF)

Confirmation and Generalization of an Alcohol-Dependence Locus on Chromosome 10q

Neuropsychopharmacology (New York, N.Y.), 2010-05, Vol.35 (6), p.1325-1332

2010

Volltextzugriff (PDF)

NOD2 CARD15 Genotype and Phenotype Differences between Ashkenazi and Sephardic Jews with Crohn's Disease

The American journal of gastroenterology, 2004-06, Vol.99 (6), p.1134-1140

2004

Volltextzugriff (PDF)

A genome scan in 260 inflammatory bowel disease‐affected relative pairs

Inflammatory bowel diseases, 2004-01, Vol.10 (1), p.15-22

2004

Volltextzugriff (PDF)

A genome scan in 260 inflammatory bowel disease‐affected relative pairs

Inflammatory bowel diseases, 2004-09, Vol.10 (5), p.513-520

2004

Volltextzugriff (PDF)

The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults

Archives of neurology (Chicago), 2004-03, Vol.61 (3), p.351

2004

Volltextzugriff (PDF)

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree

Human genetics, 2006-08, Vol.120 (1), p.31-41

2006

Volltextzugriff (PDF)

A genome-wide scan for loci linked to plasma levels of glucose and HbA1c in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

Diabetes (New York, N.Y.), 2002-03, Vol.51 (3), p.833-840

2002

Volltextzugriff (PDF)

A Genome-Wide Scan for Loci Linked to Plasma Levels of Glucose and HbA1c in a Community-Based Sample of Caucasian Pedigrees

Diabetes (New York, N.Y.), 2002-03, Vol.51 (3), p.833-840

2002

Volltextzugriff (PDF)

Parental sex effect in families with alcoholism

Genetic epidemiology, 1999, Vol.17 (S1), p.S409-S413

1999

Volltextzugriff (PDF)

Genetic Susceptibility to Asthma — Bronchial Hyperresponsiveness Coinherited with a Major Gene for Atopy

The New England journal of medicine, 1995-10, Vol.333 (14), p.894-900

1995

Volltextzugriff (PDF)

Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity

Gastroenterology (New York, N.Y. 1943), 2000-12, Vol.119 (6), p.1483-1490

2000

Volltextzugriff (PDF)

Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses

BMC genetics, 2003-12, Vol.4 Suppl 1 (S1), p.S15, Article S15

2003

Volltextzugriff (PDF)

Genome-wide screen for heavy alcohol consumption

BMC genetics, 2003-12, Vol.4 Suppl 1 (S1), p.S106, Article S106

2003

Volltextzugriff (PDF)

Search for genetic factors predisposing to atherogenic dyslipidemia

BMC genetics, 2003-12, Vol.4 Suppl 1 (S1), p.S100, Article S100

2003

Volltextzugriff (PDF)

Characterization of obstructive airway disease in family members of probands with asthma: An algorithm for the diagnosis of asthma

American journal of respiratory and critical care medicine, 1998-06, Vol.157 (6), p.1734-1742

1998

Volltextzugriff (PDF)

Two-locus approach of segregation and linkage analysis in the study of complex traits

Genetic epidemiology, 1995, Vol.12 (6), p.825-830

1995

Volltextzugriff (PDF)

A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

Diabetes (New York, N.Y.), 2002-03, Vol.51 (3), p.833-840

2002

Volltextzugriff (PDF)

Susceptibility Loci Regulating Total Serum IgE Levels, Bronchial Hyperresponsiveness, and Clinical Asthma Map to Chromosome 5q

Chest, 1997-06, Vol.111 (6), p.77S-78S

1997

Volltextzugriff (PDF)

1 – 25 von 43

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(37)

Publikationsform

Artikel
(43)

Sprache

Englisch
(43)

Erscheinungsjahr

n.n

Thema

Humans
(34)
Science & Technology
(34)
Life Sciences & Biomedicine
(33)
Female
(27)
Biological And Medical Sciences
(25)
Male
(24)
Medical Sciences
(20)
Adult
(18)
Genetics & Heredity
(16)
Middle Aged
(15)
Genetic Linkage
(14)
Genetic Predisposition To Disease
(12)
Gene Frequency
(11)
Genotype
(11)
Pedigree
(10)
Phenotype
(9)
Chromosome Mapping
(8)
Fundamental And Applied Biological Sciences. Psychology
(8)
Risk Factors
(8)
Adolescent
(7)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

The impact of race as a risk factor for symptom severity and age at diagnosis of uterine leiomyomata among affected sisters

MDR1 Ala893 Polymorphism Is Associated with Inflammatory Bowel Disease

Polymorphisms in the Insulin-Degrading Enzyme Gene Are Associated With Type 2 Diabetes in Men From the NHLBI Framingham Heart Study

Involvement of fumarate hydratase in nonsyndromic uterine leiomyomas: Genetic linkage analysis and FISH studies

Variation and heritability of Hb F and F‐cells among β‐thalassemia heterozygotes in Hong Kong

Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis

Confirmation and Generalization of an Alcohol-Dependence Locus on Chromosome 10q

NOD2 CARD15 Genotype and Phenotype Differences between Ashkenazi and Sephardic Jews with Crohn's Disease

A genome scan in 260 inflammatory bowel disease‐affected relative pairs

A genome scan in 260 inflammatory bowel disease‐affected relative pairs

The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree

A genome-wide scan for loci linked to plasma levels of glucose and HbA1c in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

A Genome-Wide Scan for Loci Linked to Plasma Levels of Glucose and HbA1c in a Community-Based Sample of Caucasian Pedigrees

Parental sex effect in families with alcoholism

Genetic Susceptibility to Asthma — Bronchial Hyperresponsiveness Coinherited with a Major Gene for Atopy

Linkage heterogeneity for the IBD1 locus in Crohn's disease pedigrees by disease onset and severity

Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses

Genome-wide screen for heavy alcohol consumption

Search for genetic factors predisposing to atherogenic dyslipidemia

Characterization of obstructive airway disease in family members of probands with asthma: An algorithm for the diagnosis of asthma

Two-locus approach of segregation and linkage analysis in the study of complex traits

A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

Susceptibility Loci Regulating Total Serum IgE Levels, Bronchial Hyperresponsiveness, and Clinical Asthma Map to Chromosome 5q

Suchergebnisse filtern