F. Pope

B. Tsai-Goodman, A. G. Stuart, F. Pope, 2002, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

Clinical phenotypes and molecular characterisation of three patients with Ehlers-Danlos syndrome type VII

M. Wright, R. Mueller, F. Pope, 2000, Journal of medical genetics.

Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndrome

T. Clark, J. Ayres, J. Reidy, 2022 .

Mutation in the carboxy‐terminal propeptide of the proα1 (I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): Possible implications for protein folding

F. Pope, A. Nicholls, E. Thompson, 1996, Human mutation.

Autosomal dominant pseudoxanthoma elasticum

F. Pope, 1974, Journal of medical genetics.

Cutaneous extensibility in pseudo‐xanthoma elasticum

W. Harvey, R. Grahame, F. Pope, 1975, The British journal of dermatology.

The Buschke–Ollendorff syndrome presenting as familial elastic tissue naevi

F. Pope, S. Woodrow, S. Handfield‐Jones, 2001, The British journal of dermatology.

A light and electron microscopic study of osteogenesis imperfecta bone samples, with reference to collagen chemistry and clinical phenotype

P. Sarathchandra, F. Pope, M. Kayser, 2000, The Journal of pathology.

Connective tissue naevus (collagenoma) in a patient with benign joint hypermobility syndrome (Ehlers–Danlos syndrome type III)

C. Bunker, R. Grahame, F. Pope, 2003, Clinical and experimental dermatology.

OUT‐PATIENT TREATMENT OF ICHTHYOSIS: A DOUBLE‐BLIND TRIAL OF OINTMENTS

F. Pope, R. Wells, J. Rees, 1972, The British journal of dermatology.

Spontaneous rupture of the femoral arteries.

F. Pope, G. Watkin, M. Cadier, 1993, Journal of the Royal Society of Medicine.

Azure lunules in Argyria. Corneal changes resembling Kayser-Fleischer Rings.

M. Whelton, F. Pope, 1968, Archives of internal medicine.

Detection of type III collagen in skin fibroblasts from patients with Ehlers‐Danlos syndrome type IV by immunofluorescence

F. Pope, P. Narcisi, A. Temple, 1988, The British journal of dermatology.

Accumulation of membrane‐bound melanosomes occurs in Langerhans cells of patients with the Leopard Syndrome

F. Pope, P. Fryer, F. Pope, 1992, Clinical and experimental dermatology.

with homozygous sickle cell disease . Angioid streaks in Jamaican patients

G. Slavin, C. Sowter, A. M. Hamilton, 2004 .

Angioid streaks in Jamaican patients with homozygous sickle cell disease.

G. Slavin, C. Sowter, A. M. Hamilton, 1981, The British journal of ophthalmology.

The prevalence of bone cysts in Darier's disease: a survey of 31 cases

R. Thomas, M. Black, C. Payne, 1984, Clinical and experimental dermatology.

Clinical variability of osteogenesis imperfecta reflecting molecular heterogeneity: cysteine substitutions in the alpha 1(I) collagen chain producing lethal and mild forms.

F. Pope, A. Nicholls, B. Steinmann, 1986, The Journal of biological chemistry.

Homozygosity for a splice site mutation of the COL1A2gene yields a non-functional proα2(I) chain and an EDS/OI clinical phenotype

S. Wallis, F. Pope, A. Nicholls, 2001, Journal of medical genetics.

BIOCHEMICAL HETEROGENEITY OF OSTEOGENESIS IMPERFECTA: NEW VARIANT

F. Pope, A. Nicholls, H. Schloon, 1979, The Lancet.

The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: Exon skipping caused by an 11-bp deletion from an intron in one COL1A2 allele

D. Heath, F. Pope, A. Nicholls, 1992, Human Genetics.

Current topic Molecular abnormalities of collagen in human disease

F. Pope, A. Nicholls, 2006 .

Prenatal diagnosis and prevention of inherited abnormalities of collagen

F. Pope, P. Narcisi, A. Nicholls, 1989, Journal of Inherited Metabolic Disease.

Genetics of inherited defects of connective tissue.

F. Pope, 1988, Bailliere's clinical rheumatology.

Molecular abnormalities of collagen in human disease.

F. Pope, A. Nicholls, 1987, Archives of disease in childhood.

Ehlers-Danlos syndrome.

F. Pope, 1991, Bailliere's clinical rheumatology.

The molecular defect in a nonlethal variant of osteogenesis imperfecta. Synthesis of pro-alpha 2(I) chains which are not incorporated into trimers of type I procollagen.

D. Prockop, F. Pope, A. Nicholls, 1983, The Journal of biological chemistry.

Ehlers–Danlos syndrome type IV mimicking non‐accidental injury in a child

D. Roberts, F. Pope, P. Narcisi, 1984, The British journal of dermatology.

Clinical, biochemical and molecular aspects of bone collagen disorders

F. Pope, A. Nicholls, 1990 .

GENETIC ENGINEERING AND GENE ANALYSIS

F. Pope, 1983, The British journal of dermatology.

Spontaneous rupture of the renal artery in a patient with Ehlers-Danlos syndrome type IV.

A. Bakka, F. Pope, I. Brekke, 1997, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.

Ehlers-Danlos syndrome hasvaried molecular mechanisms

N. Burrows, F. Pope, 1997 .

Syndrome of the month Ehlers-Danlos syndrome has varied molecular mechanisms

N. Burrows, F. Pope, 2022 .

Collagen genes and proteins in osteogenesis imperfecta.

R. Owen, P. Talmud, F. Pope, 1985, Journal of medical genetics.

The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta.

D. Prockop, J. Myers, F. Pope, 1984, Journal of medical genetics.

MOLECULAR BIOLOGY OF OSTEOGENESIS IMPERFECTA

F. Pope, 1986, The Lancet.

TWO DIFFERENT CYSTEINE SUBSTITUTIONS IN THE SAME α1(I) CB6 PEPTIDE OF THE α1(I) COLLAGEN CHAIN PRODUCE A LETHAL AND A MILD FORM OF OSTEOGENESIS IMPERFECTA (OI)

F. Pope, A. Nicholls, B. Steinmann, 1985, Pediatric Research.

Osteogenesis imperfecta: cloning of a pro-alpha 2(I) collagen gene with a frameshift mutation.

T. Pihlajaniemi, D. Prockop, J. Myers, 1984, The Journal of biological chemistry.

Lethal osteogenesis imperfecta congenita and a 300 base pair gene deletion for an alpha 1(I)-like collagen.

K. Cheah, F. Grosveld, F. Pope, 1984, British medical journal.

An abnormal collagen alpha chain containing cysteine in autosomal dominant osteogenesis imperfecta.

F. Pope, A. Nicholls, D. Craig, 1984, British medical journal.

Osteogenesis imperfecta (lethal) bones contain types III and V collagens.

J. Parkin, E. Hey, F. Pope, 1980, Journal of clinical pathology.

Molecular Abnormalities of Collagen: A Review

F. Pope, A. Nicholls, J. Dorling, 1983, Journal of the Royal Society of Medicine.

The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

N. Rahman, P. Futreal, S. Edkins, 2002, American journal of human genetics.

An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome.

D. Greenspan, F. Pope, A. Nicholls, 1996, Journal of medical genetics.

Stickler Syndrome Type 2 and Linkage to the COL11A1 Gene a

S. J. Payne, F. Pope, M. Snead, 1996, Annals of the New York Academy of Sciences.

Molecular analysis of Ehlers-Danlos syndrome type II.

F. Pope, 1991, British journal of rheumatology.

Lethal osteogenesis imperfecta and a gene deletion

F. Pope, A. Nicholls, 1984 .

Connective Tissue Disease: Molecular Pathology of the Extracellular Matrix

F. Pope, 1987 .

Cutaneous histologic features in Ehlers-Danlos syndrome: study of 21 patients.

V. McKusick, F. Pope, P. Cooper, 1979, Archives of dermatology.

Cutis laxa complicating Ehlers–Danlos syndrome type II

F. Pope, L. Ostlere, C. Holden, 1996, Clinical and experimental dermatology.

Four patients with Sillence type I osteogenesis imperfecta and mild bone fragility, complicated by left ventricular cardiac valvular disease and cardiac tissue fragility caused by type I collagen mutations

N. Moat, S. Holder, A. Lund, 2014, American journal of medical genetics. Part A.

Clinical features of an affected father and daughter with Ehlers‐Danlos syndrome type VIIB

F. Pope, A. Nicholls, M. Kwee, 1992, The British journal of dermatology.

Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review

J. Zschocke, F. Pope, D. Schnabl, 2020, Acta dermato-venereologica.

Ehlers Danlos syndrome type I with novel dental features.

P. Speight, F. Pope, H. Ranta, 1992, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Genetic linkage to the collagen α1 (V) gene (COL5A1) in two British Ehlers–Danlos syndrome families with variable type I and II phenotypes

F. Pope, N. Burrows, A. Richards, 1997, Clinical and experimental dermatology.

Type III Collagen Deficiency with Normal Phenotype 1

A. Child, F. Pope, P. Narcisi, 1983, Journal of the Royal Society of Medicine.

Clinical presentations of Ehlers Danlos syndrome type IV.

F. Pope, P. Narcisi, A. Nicholls, 1988, Archives of disease in childhood.

Platelet and coagulation studies in Ehlers‐Danlos syndrome

K. Mayne, A. Anstey, F. Pope, 1990 .

Molecular abnormalities of collagen

F. Pope, A. Nicholls, 1978 .

A Polish variant of isolated dentinogenesis imperfecta with a generalised connective tissue defect

F. Pope, A. Nicholls, K. Lee, 1989, British Dental Journal.