Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families

to connected objects

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
In: 10.1186/1471-2466-5-1

Event
Veröffentlichung
(where)
Aachen
(who)
Universitätsbibliothek der RWTH Aachen
(when)
2005
Creator
Altmüller, Janine
Seidel, Corinna
Lee, Young-Ae
Loesgen, Sabine
Bulle, Dieter
Friedrichs, Frank
Jellouschek, Heidemarie
Kelber, Julika
Keller, Angela
Schuster, Antje
Silbermann, Michael
Wahlen, Wolfgang
Wolff, Peter
Schlenvoigt, Gerhard
Rüschendorf, Franz
Nürnberg, Peter
Wjst, Matthias

DOI
10.1186/1471-2466-5-1
URN
urn:nbn:de:101:1-2020110916043907904965
Rights
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:55 PM CET

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Show original at data provider

Associated

  • Altmüller, Janine
  • Seidel, Corinna
  • Lee, Young-Ae
  • Loesgen, Sabine
  • Bulle, Dieter
  • Friedrichs, Frank
  • Jellouschek, Heidemarie
  • Kelber, Julika
  • Keller, Angela
  • Schuster, Antje
  • Silbermann, Michael
  • Wahlen, Wolfgang
  • Wolff, Peter
  • Schlenvoigt, Gerhard
  • Rüschendorf, Franz
  • Nürnberg, Peter
  • Wjst, Matthias
  • Universitätsbibliothek der RWTH Aachen

Time of origin

  • 2005

Other Objects (12)

Genome-wide linkage analysis of families with primary hyperhidrosis

Genome-wide linkage analysis of families with primary hyperhidrosis

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder

Mapping QTL Affecting Growth and Body Composition in Chicken Using Genome-Wide Linkage Analyses

Hochschulschrift

Mapping QTL Affecting Growth and Body Composition in Chicken Using Genome-Wide Linkage Analyses

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Genome-wide analyses of stallion fertility

Hochschulschrift

Genome-wide analyses of stallion fertility

Genome-wide analysis of mutually exclusive splicing

Hochschulschrift

Genome-wide analysis of mutually exclusive splicing

Genome-wide response patterns in stressed hepatocytes

Hochschulschrift

Genome-wide response patterns in stressed hepatocytes

Genome-wide mapping of the inflammation methylome

Hochschulschrift

Genome-wide mapping of the inflammation methylome

Detecting signatures of convergent evolution genome-wide

Hochschulschrift

Detecting signatures of convergent evolution genome-wide

Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

Genome-wide analysis of complex traits in cattle

Hochschulschrift

Genome-wide analysis of complex traits in cattle

Related objects