David Mansfield

Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

David Parry, Alan J. Mighell, Walid El‐Sayed et al. · The American Journal of Human Genetics · 2009 · 166 citations · Full text

Linkage Mapping in 29 Bardet–Biedl Syndrome Families Confirms Loci in Chromosomal Regions 11q13, 15q22.3–q23, and 16q21

Elspeth A. Bruford, Ruth Riise, Peter Teague et al. · Genomics · 1997 · 124 citations

Chromosome Dynamics, Linkage Mapping, Chromosomal Regions 11Q13 +10

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

T J Keen, Matthew M. Hims, Arthur B. McKie et al. · European Journal of Human Genetics · 2002 · 91 citations · Full text

Pim-1 Kinase, Protein Function, Molecular Physiology +10

A New Locus for Autosomal Dominant Familial Exudative Vitreoretinopathy Maps to Chromosome 11p12-13

Louise Downey, T J Keen, Emma Roberts et al. · The American Journal of Human Genetics · 2001 · 81 citations · Full text

Ocular Disease, Vitreous Body, Ophthalmology +5

Automation of Genetic Linkage Analysis Using Fluorescent Microsatellite Markers

David Mansfield, Alastair F. Brown, Daryll K. Green et al. · Genomics · 1994 · 80 citations

Genetic Analysis, Linkage Disequilibrium, Medicine +5