Annals of Human Genetics

On the asymptotic equivalence of allelic and trend statistic under Hardy-Weinberg equilibrium
pp. 589-589(1)
Author: Knapp, Michael

Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot-Marie-Tooth Subtype CMT2B1 in Families from North Western Africa
pp. 590-597(8)
Authors: Hamadouche, T.; Poitelon, Y.; Genin, E.; Chaouch, M.; Tazir, M.; Kassouri, N.; Nouioua, S.; Chaouch, A.; Boccaccio, I.; Benhassine, T.; De Sandre-Giovannoli, A.; Grid, D.; Lévy, N.; Delague, V.

Genetic Epidemiology of Subclinical Cardiovascular Disease in the Diabetes Heart Study
pp. 598-610(13)
Authors: Bowden, D. W.; Lehtinen, A. B.; Ziegler, J. T.; Rudock, M. E.; Xu, J.; Wagenknecht, L. E.; Herrington, D. M.; Rich, S. S.; Freedman, B. I.; Carr, J. J.; Langefeld, C. D.

Quantification of the Genetic Component of Basal C-Reactive Protein Expression in SLE Nuclear Families
pp. 611-620(10)
Authors: Rhodes, B.; Meek, J.; Whittaker, J. C.; Vyse, T. J.

A Genome-wide Scan in an Amish Pedigree with Parkinsonism
pp. 621-629(9)
Authors: Lee, S. L.; Murdock, D. G.; McCauley, J. L.; Bradford, Y.; Crunk, A.; McFarland, L.; Jiang, L.; Wang, T.; Schnetz-Boutaud, N.; Haines, J. L.

Cognitive Functioning and Survival in the Elderly: The SSADH C538T Polymorphism
pp. 630-635(6)
Authors: De Rango, F.; Leone, O.; Dato, S.; Novelletto, A.; Bruni, A. C.; Berardelli, M.; Mari, V.; Feraco, E.; Passarino, G.; De Benedictis, G.

Identification of Association of Common AGGF1 Variants with Susceptibility for Klippel-Trenaunay Syndrome Using the Structure Association Program
pp. 636-643(8)
Authors: Hu, Y.; Li, L.; Seidelmann, S. B.; Timur, A. A.; Shen, P. H.; Driscoll, D. J.; Wang, Q. K.

Correlation Analyses Reveal a Substantial Influence of Allelic Gaps on the Investigation of Genetic Diversity of Modern Human Populations with Microsatellites
pp. 644-653(10)
Authors: Guha, S.; Chakraborty, R.

Four SNPS on Chromosome 9p21 Confer Risk to Premature, Familial CAD and MI in an American Caucasian Population (GeneQuest)
pp. 654-657(4)
Authors: Abdullah, K. G.; Li, L.; Shen, G.-Q.; Hu, Y.; Yang, Y.; MacKinlay, K. G.; Topol, E. J.; Wang, Q. K.

A Bayesian Spatial Multimarker Genetic Random-Effect Model for Fine-Scale Mapping
pp. 658-669(12)
Authors: Tsai, M.-Y.; Hsiao, C. K.; Wen, S.-H.

Identifying Modifier Loci in Existing Genome Scan Data
pp. 670-675(6)
Authors: Daw, E. W.; Lu, Y.; Marian, A. J.; Shete, S.

Exact Trait-Model-Free Tests for Linkage Detection in Pedigrees
pp. 676-682(7)
Authors: Basu, S.; Di, Y.; Thompson, E. A.

HMBS Mutations in Chinese Patients with Acute Intermittent Porphyria
pp. 683-686(4)
Authors: Yang, C.-C.; Kuo, H.-C.; You, H.-L.; Wang, J.; Huang, C.-C.; Liu, C.-Y.; Lan, M.-Y.; Stephenson, D. A.; Lee, M.-J.

European Mathematical Genetics Meeting, Rotterdam, the Netherlands, 10^th-11^th April 2008
pp. 687-695(9)

Contribution of Gender-Specific Genetic Factors to Osteoporosis Risk
pp. 696-714(19)
Authors: Karasik, D.; Ferrari, S. L.

Erratum
pp. 715-715(1)