M.V. Bell

Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome

M.V. Bell, Mark C. Hirst, Yutaka Nakahori et al. · Cell · 1991 · 358 citations

Fragile X Syndrome, Developmental Biology, Clinical Expression +9

Identification and characterization of three members of the human SR family of pre-mRNA splicing factors.

Gavin Screaton, Javier F. Cáceres, Akila Mayeda et al. · The EMBO Journal · 1995 · 297 citations · Full text

Human Sr Family, Transcriptional Regulation, Pre-mrna Splicing Factors +11

The identification of a new alternative exon with highly restricted tissue expression in transcripts encoding the mouse Pgp-1 (CD44) homing receptor. Comparison of all 10 variable exons between mouse, human, and rat

Gavin Screaton, M.V. Bell, J I Bell et al. · Journal of Biological Chemistry · 1993 · 243 citations · Full text

Immunology, Pathology, Extracellular Microvesicles +17

MASA syndrome: further clinical delineation and chromosomal localisation

RobinM. Winter, KayE. Davies, M.V. Bell et al. · Human Genetics · 1989 · 65 citations

Down Syndrome, Mendelian Disorder, Genetic Disorder +6

A New DNA Marker Tightly Linked to the Fragile X Locus ( <i>FRAXA</i> )

G K Suthers, David F. Callen, V.J. Hyland et al. · Science · 1989 · 61 citations

Genetics, Genomic Mechanism, Molecular Biology +19