Clinical and genetic characteristics of hereditary pancreatitis in Europe

Nathan Howes, Markus M. Lerch, William Greenhalf, +15

Clinical Gastroenterology and Hepatology

Pancreatic Fluid CollectionGenetic EpidemiologyGastroenterologyPathologyHereditary Pancreatitis +2

The complete nucleotide sequence of a common cold virus: human rhinovlrus 14

Glyn Stanway, P. J. Hughes, Roger Mountford, +2

Nucleic Acids Research

Specific mutations in KRAS codon 12 are associated with worse overall survival in patients with advanced and recurrent colorectal cancer

Robert Jones, Paul Sutton, Jonathan Evans, +7

British Journal of Cancer

The nucleotide sequence of poliovirus type 3 leon 12 a¹b: comparison with poliovirus type 1

Glyn Stanway, Alan J. Cann, Rudolf Hauptmann, +6

Nucleic Acids Research

Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers

Jonathan Cohn, John P. Neoptolemos, Jinong Feng, +6

Human Mutation

Genetic DisorderMedicineGeneticsPathogenesisGenetic Epidemiology +11

Nemaline myopathy caused by absence of α‐skeletal muscle actin

Kristen L. Nowak, Caroline A. Sewry, Carmen Navarro, +14

Annals of Neurology

Genetic Polymorphisms and Retinopathy of Prematurity

Richard Cooke, J Drury, Roger Mountford, +1

Investigative Ophthalmology & Visual Science

The human LMX1B gene: transcription unit, promoter, and pathogenic mutations

Jennifer A. Dunston, Jeanette Hamlington, Jayshree Zaveri, +7

Genomics

Transcriptional RegulationGeneticsGenomic MechanismGene RegulationGene Characterization +6

Noncoding copy-number variations are associated with congenital limb malformation

Ricarda Flöttmann, Bjørt K. Kragesteen, Sinje Geuer, +24

Genetics in Medicine

Developmental AnomalyThumb HypoplasiaDevelopmental BiologyGenetic DisorderGenetics +4

Spectrum of factor XI (F11) mutations in the UK population – 116 index cases and 140 mutations

Michael Mitchell, Roger Mountford, Rachel Butler, +4

Human Mutation