W. Lanyon

发表

Characterisation of inherited and sporadic mutations in neurofibromatosis type-1.

S. Purandare, W. Lanyon, J. Connor, 1994, Human molecular genetics.

Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 gene.

S. Purandare, W. Lanyon, J. Connor, 1995, Human molecular genetics.

Studies on the heterogeneity of mouse-globin messenger RNA.

W. Lanyon, J. Paul, R. Williamson, 1972, European journal of biochemistry.

Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion

R. Williamson, J. Clegg, D. Weatherall, 1974, Nature.

δβ-Thalassemia is due to a gene deletion

J. Clegg, D. Weatherall, W. Lanyon, 1976, Cell.

A novel insertional mutation of a single base in exon 34 of the neurofibromatosis‐1 gene

S. Purandare, W. Lanyon, J. Connor, 1994, Human mutation.

The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1974, Nature.

Delta-beta-thalassemia is due to a gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1976, Cell.

CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.

R. MacKie, W. Lanyon, J. Connor, 1998, The Journal of investigative dermatology.

Multiple origins of transcription in the 4.5 Kb upstream of the epsilon-globin gene.

W. Lanyon, J. Paul, M. Allan, 1983, Cell.

Characterization ofAlu family repetitive sequences which flank human β-type globin genes

W. Lanyon, G. Grindlay, J. Paul, 1981, Bioscience reports.

Human globin gene analysis for a patient with beta-o/delta beta-thalassemia.

R. Williamson, J. Clegg, D. Weatherall, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Identification of a new missense point mutation in exon 4 of the Cu/Zn superoxide dismutase (SOD-1) gene in a family with amyotrophic lateral sclerosis.

W. Lanyon, J. Connor, A. Elshafey, 1994, Human molecular genetics.

The poly(adenylic acid) sequence of mouse globin messenger RNA.

W. Lanyon, J. Mansbridge, R. Williamson, 1974, European journal of biochemistry.

Characterisation of a 5-bp deletion in exon 4 of the factor VIII gene: concordance with slipped-mispairing at DNA replication

S. Bidichandani, W. Lanyon, J. Connor, 1994, Human Genetics.

The fractionation of ribonucleic acid on a preparative scale by polyacrylamide gel electrophoresis

W. Lanyon, J. Paul, R. Williamson, 1968, FEBS letters.

Alternative sites of transcription initiation upstream of the canonical cap site in human -γ-globin and β-globin genes

W. Lanyon, G. Grindlay, J. Paul, 1984 .

Human globin gene expression and linkage in bone marrow and fetal liver.

R. Williamson, W. Lanyon, S. Ottolenghi, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Characteristics of erythropoietin-induced RNA from foetal mouse liver erythropoietic cell cultures and the effects of 5-fluorodeoxyuridine.

W. Lanyon, J. Paul, R. Williamson, 1972, Biochimica et biophysica acta.

AB1 repetitive sequence near the mouse β-major globin gene

J. Vass, W. Lanyon, J. Paul, 1982 .

Tightly linked polymorphic markers for fragile X syndrome and prenatal cytogenetic diagnostic experience.

I. Glass, W. Lanyon, J. Connor, 1992, American journal of medical genetics.

A novel splice donor mutation affecting position +3 in intron 6 of the factor VIII gene.

S. Bidichandani, W. Lanyon, J. Connor, 1994, Human molecular genetics.

Detection of a high mutation frequency in exon 12 of the porphobilinogen deaminase gene in patients with acute intermittent porphyria

G. Louie, W. Lanyon, J. Connor, 1993, Human Genetics.

Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNA

W. Lanyon, J. Connor, M. Moore, 1992, Human Genetics.

Evidence for involvement of a second genetic locus on chromosome 11q in porphyrin metabolism

M. Porteous, W. Lanyon, J. Connor, 1993, Human Genetics.

Identification of Two Novel Mutations in the Hydroxymethylbilane Synthase Gene in Three Patients from Two Unrelated Families with Acute Intermittent Porphyria

W. Lanyon, J. Connor, M. Moore, 1998, Human Heredity.

Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthase.

W. Lanyon, J. Connor, M. Moore, 1997, Molecular and cellular probes.

Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.

M. Ferguson-Smith, A. McWhinnie, W. Lanyon, 1990, Journal of medical genetics.

Detection of four mutations in six unrelated South African patients with acute intermittent porphyria.

W. Lanyon, J. Connor, M. Moore, 1996, Molecular and Cellular Probes.

Identification of five novel mutations in the porphobilinogen deaminase gene.

G. Louie, W. Lanyon, J. Connor, 1994, Human Molecular Genetics.

Detection of mutations in ectopic factor VIII transcripts from nine haemophilia A patients and the correlation with phenotype

S. Bidichandani, W. Lanyon, J. Connor, 1995, Human Genetics.