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Genetic mapping

A Single Nucleotide Polymorphism within the Interferon Gamma Receptor 2 Gene Perfectly Coincides with Polledness in Holstein Cattle

Sabrina Glatzer, Nina Johanna Merten, [ ... ], Ottmar Distl

Molecular Phylogeography and Population Genetic Structure of an Endangered Species Pachyhynobius shangchengensis (hynobiid Salamander) in a Fragmented Habitat of Southeastern China

Yanyu Zhao, Yanhua Zhang, Xiaochen Li

Identification of Pummelo Cultivars by Using a Panel of 25 Selected SNPs and 12 DNA Segments

Bo Wu, Guang-yan Zhong, [ ... ], Dong-guo Zhou

Genetic and Evolutionary Analyses of the Human Bone Morphogenetic Protein Receptor 2 (BMPR2) in the Pathophysiology of Obesity

Dorit Schleinitz, Nora Klöting, [ ... ], Peter Kovacs

Neurotensin Receptor 1 Gene (NTSR1) Polymorphism Is Associated with Working Memory

Jin Li, Chuansheng Chen, [ ... ], Qi Dong

Diversity of Extended HLA-DRB1 Haplotypes in the Finnish Population

Annika Wennerström, Efthymia Vlachopoulou, [ ... ], Marja-Liisa Lokki

Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1

Laura Caleca, Anna Laura Putignano, [ ... ], Paolo Radice

Genetic Variations in HSPA8 Gene Associated with Coronary Heart Disease Risk in a Chinese Population

Meian He, Huan Guo, [ ... ], Tangchun Wu

Maternal inheritance of deltamethrin resistance in the salmon louse Lepeophtheirus salmonis (Krøyer) is associated with unique mtDNA haplotypes

Greta Carmona-Antoñanzas, Michaël Bekaert, [ ... ], Armin Sturm

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA

Jesper Buchhave Poulsen, Francesco Lescai, [ ... ], Mads Vilhelm Hollegaard

Insights into evolving global populations of Phytophthora infestans via new complementary mtDNA haplotype markers and nuclear SSRs

Frank N. Martin, Yonghong Zhang, [ ... ], William E. Fry

Molecular Characterization of the Cytidine Monophosphate-N-Acetylneuraminic Acid Hydroxylase (CMAH) Gene Associated with the Feline AB Blood Group System

Toshinori Omi, Shota Nakazawa, [ ... ], Shigenori Ikemoto

Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)

Allison J. Cox, Benjamin W. Darbro, [ ... ], Polly J. Ferguson

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