Annals of Human Genetics

A Novel Genetic Study of Chinese Families with Autosomal Recessive Retinitis Pigmentosa
pp. 281-294(14)
Authors: Abd El-Aziz, M. M.; El-Ashry, M. F.; Chan, W. M.; Chong, K. L.; Barragan, I.; Antiñolo, G.; Pang, C. P.; Bhattacharya, S. S.

The Relationship Between CAG Repeat Length and Age of Onset Differs for Huntington's Disease Patients with Juvenile Onset or Adult Onset
pp. 295-301(7)
Authors: Andresen, J. Michael; Gayán, Javier; Djoussé, Luc; Roberts, Simone; Brocklebank, Denise; Cherny, Stacey S.; Cardon, Lon R.; Gusella, James F.; MacDonald, Marcy E.; Myers, Richard H.; Housman, David E.; Wexler, Nancy S.

Osteoprotegerin Plasma Levels are Strongly Associated with Polymorphisms in Human Homologue of the Mouse Progressive Ankylosis (ANKH) Gene
pp. 302-307(6)
Authors: Vistoropsky, Y.; Malkin, I.; Kobyliansky, E.; Livshits, G.

Association of a Common Interferon Regulatory Factor 5 (IRF5) Variant with Increased Risk of Systemic Lupus Erythematosus (SLE)
pp. 308-311(4)
Authors: Demirci, F. Y. K.; Manzi, S.; Ramsey-Goldman, R.; Minster, R. L.; Kenney, M.; Shaw, P. S.; Dunlop-Thomas, C. M.; Kao, A. H.; Rhew, E.; Bontempo, F.; Kammerer, C.; Kamboh, M. I.

Correlation between single nucleotide polymorphisms in a calprotectin subunit gene and risk of periodontitis in a Chinese population
pp. 312-324(13)
Authors: Li, QiYan; Meng, HuanXin; Zhang, Li; Xu, Li; Chen, ZhiBin; Shi, Dong; Feng, XiangHui; Zhu, XiaoLing; Zhao, HongShan; Cao, CaiFang

Common Polymorphisms in the CACNA1H Gene Associated with Childhood Absence Epilepsy in Chinese Han Population
pp. 325-335(11)
Authors: Liang, J.; Zhang, Y.; Chen, Y.; Wang, J.; Pan, H.; Wu, H.; Xu, K.; Liu, X.; Jiang, Y.; Shen, Y.; Wu, X.

Carrier Frequency of a Nonsense Mutation in the Adenosine Deaminase (ADA) Gene Implies a High Incidence of ADA-deficient Severe Combined Immunodeficiency (SCID) in Somalia and a Single, Common Haplotype Indicates Common Ancestry
pp. 336-347(12)
Authors: Sanchez, Juan J.; Monaghan, Gemma; Børsting, Claus; Norbury, Gail; Morling, Niels; Gaspar, H. Bobby

Congenital Disorder of Glycosylation Type Ia: Searching for the Origin of Common Mutations in PMM2
pp. 348-353(6)
Authors: Quelhas, D.; Quental, R.; Vilarinho, L.; Amorim, A.; Azevedo, L.

Signatures of Positive Selection in Genes Associated with Human Skin Pigmentation as Revealed from Analyses of Single Nucleotide Polymorphisms
pp. 354-369(16)
Authors: Lao, O.; de Gruijter, J. M.; van Duijn, K.; Navarro, A.; Kayser, M.

A Comparison of the Variability Spectra of Two Genomic Loci in a European Group of Individuals Reveals Fundamental Differences Pointing to Selection or a Population Bottleneck
pp. 370-378(9)
Authors: Schmegner, C.; Hoegel, J.; Vogel, W.; Assum, G.

The Gagauz, a Linguistic Enclave, are not a Genetic Isolate
pp. 379-389(11)
Authors: Nasidze, Ivan; Quinque, Dominique; Udina, Irina; Kunizheva, Svetlana; Stoneking, Mark

Extreme Patterns of Variance in Small Populations: Placing Limits on Human Y-Chromosome Diversity through Time in the Vanuatu Archipelago
pp. 390-406(17)
Author: Cox, M.

A Markov Chain Monte Carlo Method for Estimating Population Mixing Using Y-chromosome Markers: Mixing of the Han People in China
pp. 407-420(14)
Authors: Jow, H.; Amos, W.; Luo, H.; Zhang, Y.; Burroughs, N. J.