Volume 77, Issue 1
Articles
- Diane M. Warren, Jose Manuel Soria, Juan Carlos Souto, and Anthony Comuzzie
Heritability of Hemostasis Phenotypes and Their Correlation with Type 2 Diabetes Status in Mexican Americans - Laura Almasy, David I. Rainwater, Shelley Cole, and Michael C. Mahaney
Joint Linkage and Association Analysis of the Hepatic Lipase Promoter Polymorphism and Lipoprotein Size Phenotypes - Yoshiji Yamada, Fujilo Ando, Naoakira niino, and Hiroshi Shimokata
Association of a 1997GVT Polymorphism of the Collagen I 1 Gene with Bone Mineral Density in Postmenopausal Japanese Women - Claudia C. Branco and Luisa Mota-Vieira
Surnames in the Azores: Analysis of the Isonymy Structure - A Tagarelli, A Prio, G Tagarelli, and P Lagonia
Genetic Characterization of the Historical Albanian Ethnic Minority of Calabria (Southern Italy) - Lotfi Cherni, Besma Yaacoubi Loueslati, Luisa Pereira, and Hajer Ennafaa
Female Gene Pools of Berber and Arab Neighboring Communities in Central Tunisia: Microstructure of mtDNA Variation in North Africa - Edward A. Ruiz-Narvaez, Fabricio R. Santos, Denise R. Carvalho-Silva, and Jorge Azofeifa
Genetic Variation of the Y Chromosome in Chibcha-Speaking Amerindians of Costa Rica and Panama - Tatiana M. Karafet, J S. Lansing, Alan J. Redd, and Svetlana Reznikova
Balinese Y-Chromosome Perspective on the Peopling of Indonesia: Genetic Contributions from Pre-Neolithic Hunter- Gatherers, Austronesian Farmers, and Indian Traders - Olga Rickards, Cristina Martinez-Labarga, Emiliano Trucchi, and Fabio Renzi
Restriction Fragment Length Polymorphisms of Type I Collagen Locus 2 (COL1A2) in Two Communities of African Ancestry and Other Mixed Populations of Northwestern Ecuador - Giselda M. K. Cabello, Pedro H. Cabello, Koko Otsuki, and Maria Emilia Gombarovits
Molecular Analysis of 23 Exons of the CFTR Gene in Brazilian Patients Leads to the Finding of Rare Cystic Fibrosis Mutations - Yvette Curlis, Cuiling Zhang, Jeanette J. A. Holden, and Ken Kirkby
Haplotype Study of Intermediate-Length Alleles at the Fragile X (FMR1) Gene: ATL1, FMRb, and Microsatellite Haplotypes Differ from Those Found in Common-Size FMR1 Alleles
