Annals of Human Genetics

Phenotype Severity and Genetic Variation at the Disease Locus: An Investigation of Nail Dysplasia in the Nail Patella Syndrome
pp. 1-8(8)
Authors: Dunston, J. A.; Lin, S.; Park, J. W.; Malbroux, M.; McIntosh, I.

Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
pp. 9-14(6)
Authors: Seeman, P.; Bendová, O.; Raková, D.; Malíková, M.; Groh, D.; Kabelka, Z.

Comprehensive Cystic Fibrosis Mutation Epidemiology and Haplotype Characterization in a Southern Italian Population
pp. 15-24(10)
Authors: Castaldo, G.; Polizzi, A.; Tomaiuolo, R.; Cazeneuve, C.; Girodon, E.; Santostasi, T.; Salvatore, D.; Raia, V.; Rigillo, N.; Goossens, M.; Salvatore, F.

The Contribution of Genetic and Environmental Factors to Quantitative Variability of Erythrocyte Membrane Proteins in Primary Hypotension
pp. 25-35(11)
Authors: Ivanov, V. P.; Polonikov, A. V.; Solodilova, M. A.

2-Adrenergic Receptor Gene Variations Associated with Stage-2 Hypertension in Northern Han Chinese
pp. 36-44(9)
Authors: Ge, D.; Huang, J.; He, J.; Li, B.; Duan, X.; Chen, R.; Gu, D.

Linkage Analysis of Chromosome 1 with Essential Hypertension and Blood Pressure Quantitative Traits in Chinese Families
pp. 45-54(10)
Authors: Ge, D.; Huang, J.; Yang, W.; Zhao, J.; Shen, Y.; Qiang, B.; Gu, D.

Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration
pp. 55-66(12)
Authors: Makhoul, N. J.; Wells, R. S.; Kaspar, H.; Shbaklo, H.; Taher, A.; Chakar, N.; Zalloua, P. A.

Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups
pp. 67-89(23)
Authors: Starikovskaya, Elena B.; Sukernik, Rem I.; Derbeneva, Olga A.; Volodko, Natalia V.; Ruiz-Pesini, Eduardo; Torroni, Antonio; Brown, Michael D.; Lott, Marie T.; Hosseini, Seyed H.; Huoponen, Kirsi; Wallace, Douglas C.

Genetic Association Studies in Complex Disease: Disentangling Additional Predisposing Loci from Associated Neutral Loci Using a Constrained - Permutation Approach
pp. 90-101(12)
Authors: Spijker, G.T.; Nolte, I.M.; Jansen, R.C.; Te Meerman, G.J.

Fine Mapping Functional Sites or Regions from Case-Control Data Using Haplotypes of Multiple Linked SNPs
pp. 102-112(11)
Authors: Cheng, Rong; Ma, Jennie Z.; Elston, Robert C.; Li, Ming D.

Linkage Analysis of Affected Sib Pairs Allowing for Parent-of-Origin Effects
pp. 113-126(14)
Authors: Wu, Chih-Chieh; Shete, Sanjay; Amos, Christopher I.

The use of Allelic Expression Differences to Ascertain Functional Polymorphisms Acting in cis: Analysis of MMP1 Transcripts in Normal Lung Tissue
pp. 127-133(7)
Authors: Heighway, J.; Bowers, N. L.; Smith, S.; Betticher, D. C.; Santibáñez Koref, M. F.

Corrigendum
pp. 134-134(1)