Annals of Human Genetics

Exploration of Multilocus Effects in a Highly Polymorphic Gene, the Apolipoprotein (APOB) Gene, in Relation to Plasma apoB Levels
pp. 405-418(14)
Authors: N. Tahri-Daizadeh; D. A. Tregouet; V. Nicaud; O. Poirier; F. Cambien; L. Tiret

Contribution of Chromosome 1q21-q23 to Familial Combined Hyperlipidemia in Mexican Families
pp. 419-427(9)
Authors: A. Huertas-Vázquez; J. P. del Rincón; S. Canizales-Quinteros; L. Riba; G. Vega-Hernández; S. Ramírez-Jiménez; M. Aurón-Gómez; F. J. Gómez–Pérez; C. A. Aguilar-Salinas; M. T. Tusié-Luna

Compound haplotypes at Xp11.23 and human population growth in Eurasia
pp. 428-437(10)
Authors: S. Alonso; J. A. L. Armour

Y Chromosome and Mitochondrial DNA Variation in Lithuanians
pp. 438-452(15)
Authors: D. Kasperaviit; V. Kuinskas; M. Stoneking

Mitochondrial DNA Diversity in Tribal and Caste Groups of Maharashtra (India) and its Implication on Their Genetic Origins
pp. 453-460(8)
Authors: M. M. Baig; A. A. Khan; K. M. Kulkarni

Inferring the Most Likely Geographical Origin of mtDNA Sequence Profiles
pp. 461-471(11)
Authors: T. Egeland; H.M. Bøvelstad; G.O. Storvik; A. Salas

Genetic Dissection of Human Stature in a Large Sample of Multiplex Pedigrees
pp. 472-488(17)
Authors: Yao-Zhong Liu; Fu-Hua Xu; Hui Shen; Yong-Jun Liu; Lan-Juan Zhao; Ji-Rong Long; Yuan-Yuan Zhang; Peng Xiao; Dong-Hai Xiong; Volodymyr Dvornyk; Jin-Long Li; Theresa Conway; K. Michael Davies; Robert R. Recker; Hong-Wen Deng

Commingling Analysis of Intraocular Pressure and Glaucoma in an Older Australian Population
pp. 489-497(9)
Authors: Ananth C. Viswanathan; Roger A. Hitchings; Andrea Indar; Paul Mitchell; Paul R. Healey; Peter McGuffin; Pak C. Sham

Methods for testing familial aggregation of diseases in population-based samples: application to hodgkin lymphoma in swedish registry data
pp. 498-508(11)
Authors: R. M. Pfeiffer; L. R. Goldin; N. Chatterjee; S. Daugherty; K. Hemminki; D. Pee; L. I. X; M. H. Gail

Novel HMBS founder mutation and significant intronic polymorphism in Spanish patients with acute intermittent porphyria
pp. 509-514(6)
Authors: E. Guillén-Navarro; P. Carbonell; G. Glover; M. Sánchez-Solís; A. Fernández-Barreiro

Estimated Frequency of Genetic and Nongenetic Causes of Congenital Idiopathic Cerebral Palsy in West Sweden
pp. 515-520(6)
Author: H. Costeff