The Sunday Papers (15 January 2006 edition)
Kyttala et al.
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome
Peisajovich et al.
Evolution of new protein topologies through multistep gene rearrangements
Grant et al.
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
Malek et al.
Physiogenomic resources for rat models of heart, lung and blood disorders
Smith et al.
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Comments welcome.
