Annals of Human Genetics

The MTHFD1 Gene is not Involved in Cleft Lip with or Without Palate Onset Among the Italian Population
pp. 297-299(3)
Authors: Palmieri, A.; Masiero, E.; Martinelli, M.; Scapoli, L.; Pezzetti, F.; Caramelli, E.; Guidotti, L.; Carinci, F.

Age of SERPINA1 Gene PI Z Mutation: Swedish and Latvian Population Analysis
pp. 300-304(5)
Authors: Lace, B.; Sveger, T.; Krams, A.; Cernevska, G.; Krumina, A.

A Mutation Analysis of the Phenylalanine Hydroxylase (PAH) Gene in the Israeli Population
pp. 305-309(5)
Authors: Bercovich, D.; Elimelech, A.; Yardeni, T.; Korem, S.; Zlotogora, J.; Gal, N.; Goldstein, N.; Vilensky, B.; Segev, R.; Avraham, S.; Loewenthal, R.; Schwartz, G.; Anikster, Y.

Reconstructing the Genealogy of a BRCA1 Founder Mutation by Phylogenetic Analysis
pp. 310-318(9)
Authors: Marroni, F.; Cipollini, G.; Peissel, B.; D'Andrea, E.; Pensabene, M.; Radice, P.; Caligo, M. A.; Presciuttini, S.; Bevilacqua, G.

Genomewide Linkage Scan for Combined Obesity Phenotypes using Principal Component Analysis
pp. 319-326(8)
Authors: He, L.-N.; Liu, Y.-J.; Xiao, P.; Zhang, L.; Guo, Y.; Yang, T.-L.; Zhao, L.-J.; Drees, B.; Hamilton, J.; Deng, H.-Y.; Recker, R. R.; Deng, H.-W.

Significant Association Between TIM1 Promoter Polymorphisms and Protection Against Cerebral Malaria in Thailand
pp. 327-336(10)
Authors: Nuchnoi, P.; Ohashi, J.; Kimura, R.; Hananantachai, H.; Naka, I.; Krudsood, S.; Looareesuwan, S.; Tokunaga, K.; Patarapotikul, J.

Migration Waves to the Baltic Sea Region
pp. 337-348(12)
Authors: Lappalainen, T.; Laitinen, V.; Salmela, E.; Andersen, P.; Huoponen, K.; Savontaus, M.-L.; Lahermo, P.

Mitochondrial DNA Variation in Karkar Islanders
pp. 349-367(19)
Authors: Ricaut, F. X.; Thomas, T.; Arganini, C.; Staughton, J.; Leavesley, M.; Bellatti, M.; Foley, R.; Mirazon Lahr, M.

Perturbation Analysis: A Simple Method for Filtering SNPs with Erroneous Genotyping in Genome-Wide Association Studies
pp. 368-374(7)
Authors: Teo, Y. Y.; Small, K. S.; Clark, T. G.; Kwiatkowski, D. P.

Optimal Two-Stage Design for Case-Control Association Analysis Incorporating Genotyping Errors
pp. 375-387(13)
Authors: Zuo, Y.; Zou, G.; Wang, J.; Zhao, H.; Liang, H.

EMK: A Novel Program for Family-Based Allelic and Genotypic Association Tests on Quantitative Traits
pp. 388-396(9)
Authors: Li, Y. W.; Martin, E. R.; Li, Y. J.

Efficient Approximation of P-value of the Maximum of Correlated Tests, with Applications to Genome-Wide Association Studies
pp. 397-406(10)
Authors: Li, Qizhai; Zheng, Gang; Li, Zhaohai; Yu, Kai

A Note on Allelic Tests in Case-Control Association Studies
pp. 407-409(3)
Authors: Guedj, M.; Nuel, G.; Prum, B.

Exon Deletion in the Non-catalytic Domain of eIF2Bɛ Due to a Splice Site Mutation Leads to Infantile Forms of CACH/VWM with Severe Decrease of eIF2B GEF Activity
pp. 410-415(6)
Authors: Horzinski, L.; Gonthier, C.; Rodriguez, D.; Scherer, C.; Boespflug-Tanguy, O.; Fogli, A.

Charcot-Marie-Tooth Disease: A Clinico-genetic Confrontation
pp. 416-441(26)
Authors: Barisic, N.; Claeys, K. G.; Sirotković-Skerlev, M.; Löfgren, A.; Nelis, E.; De Jonghe, P.; Timmerman, V.