Genomewide Linkage Analysis of Quantitative Spirometric Phenotypes in Severe Early-Onset Chronic Obstructive Pulmonary Disease

This publication has 39 references indexed in Scilit:

• Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes
  Human Molecular Genetics, 2002
• A Second-Generation Genomewide Screen for Asthma-Susceptibility Alleles in a Founder Population
  American Journal of Human Genetics, 2000
• Structural Organization of the Microsomal Glutathione S-Transferase Gene (MGST1) on Chromosome 12p13.1–13.2
  Published by Elsevier ,2000
• Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination
  American Journal of Human Genetics, 1998
• Approaches and issues in defining asthma and associated phenotypes map to chromosome susceptibility areas in large Minnesota families
  Clinical and Experimental Allergy, 1998
• Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
  Nature Genetics, 1995
• Neutrophil-activating peptide-1/interleukin 8, a novel cytokine that activates neutrophils.
  Journal of Clinical Investigation, 1989
• Asymptotic Properties of Maximum Likelihood Estimators and Likelihood Ratio Tests under Nonstandard Conditions
  Journal of the American Statistical Association, 1987
• Alpha1antitrypsin deficiency: The clinical and physiological features of pulmonary emphysema in subjects homozygous for Pi type Z
  Respiratory Medicine, 1983
• Ventilatory functions of normal children and young adults—Mexican-American, white, and black. I. Spirometry
  The Journal of Pediatrics, 1979