Annals of Human Genetics

Approaches to Handling Incomplete Data in Family-based Association Testing
pp. 141-151(11)
Authors: Van Steen, K.; Laird, N. M.; Markel, P.; Molenberghs, G.

Epistatic Interactions between Genomic Regions Containing the COL1A1 Gene and Genes Regulating Osteoclast Differentiation may Influence Femoral Neck Bone Mineral Density
pp. 152-159(8)
Authors: Yang, Tie-Lin; Shen, Hui; Xiong, Dong-Hai; Xiao, Peng; Guo, Yan; Guo, Yan-fang; Liu, Yao-Zhong; Recker, Robert R.; Deng, Hong-Wen

Interrelationship and Familiality of Dyslexia Related Quantitative Measures
pp. 160-175(16)
Authors: Schulte-Körne, G.; Ziegler, A.; Deimel, W.; Schumacher, J.; Plume, E.; Bachmann, C.; Kleensang, A.; Propping, P.; Nöthen, M. M.; Warnke, A.; Remschmidt, H.; König, I. R.

Polymorphisms in the Angiotensin Converting Enzyme Gene and Growth in the First Year of Life
pp. 176-184(9)
Authors: Hindmarsh, P. C.; Rodeck, C. H.; Humphries, S. E.

Molecular Epidemiology of Phenylalanine Hydroxylase Deficiency in Southern Italy: a 96% Detection Rate with Ten Novel Mutations
pp. 185-193(9)
Authors: Daniele, A.; Cardillo, G.; Pennino, C.; Carbone, M. T.; Scognamiglio, D.; Correra, A.; Pignero, A.; Castaldo, G.; Salvatore, F.

Spectrum of Mutations in the CFTR Gene in Cystic Fibrosis Patients of Spanish Ancestry
pp. 194-201(8)
Authors: Alonso, M. J.; Heine-Suñer, D.; Calvo, M.; Rosell, J.; Giménez, J.; Ramos, M. D.; Telleria, J. J.; Palacio, A.; Estivill, X.; Casals, T.

The Fate of 12 Recessive Mutations in A Single Village
pp. 202-208(7)
Authors: Zlotogora, J.; Hujerat, Y.; Barges, S.; Shalev, S. A.; Chakravarti, A.

Unbiased Interpretation of Haplotypes at Duplicated Microsatellites
pp. 209-219(11)
Authors: Balaresque, P.; Sibert, A.; Heyer, E.; Crouau-Roy, B.

A Two-Stage Approach to the Correction of Ascertainment Bias in Complex Genetic Studies Involving Variance Components
pp. 220-229(10)
Authors: Bowden, J.; Thompson, J. R.; Burton, P. R.

Mixed-effects Logistic Approach for Association Following Linkage Scan for Complex Disorders
pp. 230-237(8)
Authors: Xu, H.; Shete, S.

Analysis of Case-Only Studies Accounting for Genotyping Error
pp. 238-248(11)
Author: Cheng, K. F.

The Effects of SNP Genotyping Errors on the Power of The Cochran-Armitage Linear Trend Test for Case/Control Association Studies
pp. 249-261(13)
Authors: Ahn, Kwangmi; Haynes, Chad; Kim, Wonkuk; Fleur, Rose St.; Gordon, Derek; Finch, Stephen J.

Computing power in case-control association studies through the use of quadratic approximations: application to meta-statistics
pp. 262-270(9)
Authors: Guedj, M.; Della-Chiesa, E.; Picard, F.; Nuel, G.

Localization of a Novel Autosomal Recessive Non-syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3-q13.4
pp. 271-275(5)
Authors: Tlili, A.; Masmoudi, S.; Dhouib, H.; Bouaziz, S.; Rebeh, I. Ben; Chouchen, J.; Turki, K.; Benzina, Z.; Charfedine, I.; Drira, M.; Ayadi, H.

The Art of Reading Sequence Electropherograms
pp. 276-278(3)
Author: Parson, W.

Reply to Parson
pp. 279-280(2)
Authors: Stoneking, M.; Nasidze, I.

Editorial Note
pp. 280-280(1)