S. Bundey

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Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene.

A. Harding, M. Brockington, J. Winer, 1993, The Quarterly journal of medicine.

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.

K. Steel, T. Cole, R. Mueller, 1999, American journal of human genetics.

EARLY DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY

D. Gardner-Medwin, S. Bundey, S. Green, 1978, The Lancet.

Duplication of the 15q11‐13 Region in a Patient with Autism, Epilepsy and Ataxia

J. Corbett, C. Hardy, M. Kilpatrick, 1994, Developmental medicine and child neurology.

Dementia, epilepsy and miscellaneous disorders

S. Bundey, 1985 .

A genetic study of torsion dystonia.

C. Marsden, Marsden Cd, S. Bundey, 1975, Journal of medical genetics.

Extrapyramidal disorders and dyskinesias

S. Bundey, 1985 .

Survivors of neuroblastoma and ganglioneuroma and their families.

S. Bundey, K. Evans, 1982, Journal of medical genetics.

Tuberous sclerosis: a genetic study.

S. Bundey, K. Evans, 1969, Journal of neurology, neurosurgery, and psychiatry.

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

M. Preece, A. Green, S. Bundey, 1998, Journal of medical genetics.

Mitochondrial abnormalities in the DIDMOAD syndrome

A. Fielder, H. Whitwell, K. Poulton, 1992, Journal of Inherited Metabolic Disease.

Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy

S. Bundey, S. Mitchell, 1997, Clinical genetics.

Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.

M. Ferguson-Smith, J. Renwick, S. Bundey, 1971, Journal of medical genetics.

10 – Spastic paraplegias

S. Bundey, 1985 .

8 – Hereditary neuropathies

S. Bundey, 1985 .

Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregaria.

P. Dean, R. Dillon, A. Charnley, 2003, Archives of insect biochemistry and physiology.

Serum creatine kinase levels in pubertal, mature, pregnant, and postmenopausal women.

J. Edwards, S. Bundey, J. Crawley, 1979, Journal of medical genetics.

Muscle disorders II

S. Bundey, 1985 .

Multiple mutation in an extended Duchenne muscular dystrophy family.

D. Jadayel, A. Miciak, S. Bundey, 1992, Journal of medical genetics.

The inheritance of otosclerosis

S. Bundey, A. Morrison, 1970, The Journal of Laryngology & Otology.

Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

D. Collier, D. Curtis, M. Arranz, 1996, American journal of human genetics.

The Hereditary Ataxias and Related Disorders

S. Bundey, 1985 .

Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA).

R. Spritz, M. Musarella, K. Strunk, 1993, American journal of human genetics.

Early recognition of heterozygotes for the gene for dystrophia myotonica

C. Carter, J. Soothill, S. Bundey, 1970, Journal of neurology, neurosurgery, and psychiatry.

Recurrence risks in severe undiagnosed mental deficiency.

C. Carter, S. Bundey, 2008, Journal of mental deficiency research.

A study of retinitis pigmentosa in the City of Birmingham. I Prevalence.

S. Crews, S. Bundey, 1984, Journal of medical genetics.

Spinal muscular atrophies (SMAs)

S. Bundey, 1985 .

Huntington's Chorea

S. Bundey, 1983 .

Multifactorial inheritance and neurological diseases

S. Bundey, 1985 .

Muscle disorders I

S. Bundey, 1985 .

Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).

D. Harnden, S. Bundey, J. Morten, 1982, Journal of medical genetics.

The median survival time in open spina bifida

S. Bundey, 1997 .

Recurrence Risk of Symmetrical Spastic Cerebral Palsy

J. Young, S. Bundey, M. Griffiths, 1978, Developmental medicine and child neurology.

Phacomatoses and tumours

S. Bundey, 1985 .

A genetic study of infantile and juvenile myasthenia gravis

S. Bundey, 1972, Journal of neurology, neurosurgery, and psychiatry.

Malformations of the central nervous system

S. Bundey, 1985 .

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.

R. Spritz, R. Laxová, R. Nicholls, 1994, The New England journal of medicine.

THE SIGNIFICANCE OF A WHITE MACULE ON THE SKIN OF A CHILD

S. Bundey, 1970, Developmental medicine and child neurology.

Recurrence Risks in Families of Children with Symmetrical Spasticity

S. Bundey, M. Griffiths, 1977, Developmental medicine and child neurology.

Unusual features in the inheritance of ataxia telangiectasia

A. Taylor, C. Woods, S. Bundey, 1990, Human Genetics.

Neurological diseases in which there are defects in DNA repair or synthesis

S. Bundey, 1985 .

Genetic factors in neurological disease: tuberous sclerosis.

S. Bundey, 1971, Proceedings of the Royal Society of Medicine.

Concordance in a sample of index cases and their monozygous twins and in the population of monozygous twin pairs.

G. Chase, S. Bundey, 1972, Lancet.

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome

T. Barrett, A. Macleod, S. Bundey, 1995, The Lancet.

Wolfram syndrome: mitochondrial disorder

A. Fielder, J. Lilleyman, K. Poulton, 1993, The Lancet.

Cerebral degenerative disorders of childhood

S. Bundey, 1985 .

Are abortions more or less frequent once prenatal diagnosis is available?

S. Bundey, E. Boughton, 1989, Journal of medical genetics.

Population Screening for Genetic Disorders

S. Bundey, 1991 .

Very early onset Huntington's disease: genetic mechanism and risk to siblings

D. Clarke, S. Bundey, 1990, Clinical genetics.

Early-onset dystrophia myotonica.

C. Carter, S. Bundey, 1972, Lancet.

Genetic heterogeneity for dystrophia myotonica.

C. Carter, S. Bundey, 1972, Journal of medical genetics.

A Five-Year Prospective Study of the Health of Children in Different Ethnic Groups, with Particular Reference to the Effect of Inbreeding

S. Bundey, H. Alam, 1993, European journal of human genetics : EJHG.

Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.

A. Markham, N. Lench, R. Mueller, 1998, American journal of human genetics.

A mutation in the Norrie disease gene (NDP) associated with X–linked familial exudative vitreoretinopathy

A. Fielder, X. Breakefield, I. Craig, 1993, Nature genetics.

Allan-Herndon syndrome--or X-linked cerebral palsy?

L. Comley, S. Bundey, A. Blair, 1991, American journal of human genetics.

Clinical and Genetic Features of Ataxia-telangiectasia.

S. Bundey, 1994, International journal of radiation biology.

Clinical and genetic features of ataxia-telangiectasia.

S. Bundey, 1994, International journal of radiation biology.

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families

D. Hill, A. Chapelle, K. Davies, 2004, Human Genetics.

Birth Defects: Original Article Series, VII, 1

S. Bundey, 1972 .

Low segregation ratios in autosomal recessive disorders.

I. Young, S. Bundey, 1993, Journal of medical genetics.

A family with three sisters with the 4p- syndrome, originally reported as suffering from the Smith-Lemli-Opitz syndrome.

S. Bundey, M. Creasy, S. Hill, 2008, Journal of mental deficiency research.

RECURRANCE OF CEREBRAL PALSY — an account of a study in the West Midlands

S. Bundey, M. Griffiths, 2009 .

Uses and limitations of twin studies

S. Bundey, 1991, Journal of Neurology.

Cerebellar and spinocerebellar ataxias

S. Bundey, 1985 .

Three sisters with the Smith-Lemli-Opitz syndrome.

S. Bundey, H. Smyth, 2008, Journal of mental deficiency research.

Detection of heterozygotes for myotonic dystrophy

S. Bundey, 1974, Clinical genetics.

Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

A. Bird, M. Jay, A. Wright, 1994, Journal of medical genetics.

Immunological studies in patients with juvenile-onset myasthenia gravis and in their relatives.

D. Doniach, J. Soothill, S. Bundey, 1972, Clinical and experimental immunology.

Race, consanguinity and social features in Birmingham babies: a basis for prospective study.

R. Lancashire, S. Bundey, S. Mir, 1990, Journal of epidemiology and community health.

New mutations in Huntington's chorea.

S. Bundey, 1983, Journal of medical genetics.

Racial distribution of Duchenne muscular dystrophy in the West Midlands region of Britain.

S. Bundey, A. Roddie, 1992, Journal of medical genetics.

A Prospective Study on the Health of Birmingham Babies in Different Ethnic Groups: Interim Findings

S. Bundey, 1992 .

Why do UK-born Pakistani babies have high perinatal and neonatal mortality rates?

R. Lancashire, R. Lancashire, S. Bundey, 1991, Paediatric and perinatal epidemiology.

Spontaneous expression of the chromosome fragile site fra(10)(q25).

A. M. Taylor, S. Bundey, 1983, American journal of human genetics.

A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24.

A. Markham, D. Campbell, N. Lench, 1998, American journal of human genetics.

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

K. Davies, A. Read, T. Flint, 1988, Journal of medical genetics.

Natural history of idiopathic torsion dystonia.

C. Marsden, Marsden Cd, S. Bundey, 1976, Advances in neurology.

Large Electroencephalographic Responses and Their Relationship to Cleido-Cranial Dysplasia

S. Bundey, A. Upton, S. Sanders, 1974, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Fetal and Perinatal Neurology

S. Bundey, 1992 .

A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity.

S. Crews, S. Bundey, 1984, Journal of medical genetics.

A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity.

S. Crews, S. Bundey, 1984, Journal of medical genetics.

Clinical evidence for heterogeneity in myotonic dystrophy.

S. Bundey, 1982, Journal of medical genetics.

Ten Years Experience of a Genetic Eye Clinic: 1978–1987

S. Crews, S. Bundey, 1989, Journal of the Royal Society of Medicine.

Adrenoleucodystrophy: a molecular genetic study in five families.

M. Kilpatrick, R. D. Del Mastro, S. Bundey, 1990, Journal of medical genetics.

Myotonic dystrophy — Early detection and genetic counselling

S. Bundey, 1982, Journal of Neurology.

A clinical and genetic study of chronic proximal spinal muscular atrophy.

R. Lovelace, S. Bundey, 1975, Brain : a journal of neurology.

Wolfram (DIDMOAD) syndrome.

T. Barrett, S. Bundey, 1997, Journal of medical genetics.

Wolfram (DIDMOAD) syndrome.

T. Barrett, S. Bundey, Barrett Opl Atoh Frm, 1997, Journal of medical genetics.

DIDMOAD syndrome; further studies and muscle biochemistry

T. Barrett, K. Poulton, S. Bundey, 1995, Journal of Inherited Metabolic Disease.

The representation of ethnic minorities at genetic clinics in Birmingham.

A. Roberts, S. Bundey, R. Cullen, 1996, Journal of medical genetics.

Attitudes of 40-year-old college graduates towards amniocentesis.

S. Bundey, 1978, British medical journal.

An unusual pedigree with retinoblastoma. Does it shed light on the delayed mutation and host resistance theories?

S. Bundey, J. Morten, 2004, Human Genetics.

Optic atrophy in Wolfram (DIDMOAD) syndrome

A. Fielder, T. Barrett, P. Good, 1997, Eye.

Genetics and Neurology

S. Bundey, 1992 .

A genetic study of subacute and chronic spinal muscular atrophy in childhood A nosological analysis of 124 index patients

C. Carter, J. Pearn, J. Walton, 1978, Journal of the Neurological Sciences.

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

K. Steel, D. Trump, S. Brown, 1998, American journal of human genetics.

DIDMOAD SYNDROME - CONFIRMATION OF LINKAGE TO CHROMOSOME-4P, EVIDENCE FOR LOCUS HETEROGENEITY AND A PATIENT WITH UNIPARENTAL ISODISOMY FOR CHROMOSOME-49

D. Collier, D. Curtis, T. Barrett, 1995 .

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

C. Woods, A. Markham, D. Campbell, 1999, American journal of human genetics.

Julia Bell MRCS LRCP FRCP (1879–1979). Steamboat Lady, Statistician and Geneticist

S. Bundey, 1996, Journal of Medical Biography.

ERG and EOG abnormalities in carriers of X-linked retinitis pigmentosa

A R Fielder, S J Crews, A. Fielder, 1996, Eye.

chorea . New mutations in Huntington ' s

J. Heimans, S. Bundey, D. LINDHOUTt, 2022 .

Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom.

S. Bundey, 1978, Journal of Medical Genetics.

Insulin levels in myotonic dystrophy.

S. Bundey, 1968, The New England journal of medicine.

Is there an X‐linked form of congenital cataracts?

S. Crews, S. Bundey, 1982, Clinical genetics.

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.

H. J. Evans, M. Jay, S. Bhattacharya, 1994, American journal of human genetics.

Heterogeneity Analysis in40X-LinkedRetinitis Pigmentosa Families

M. Jay, M. Dempster, A. Carothers, 1994 .

Adult coeliac disease and neuropathy.

S. Bundey, 1967, Lancet.

The recurrence risks for mild idiopathic mental retardation.

S. Bundey, S. Bundey, A. Thake, 1989, Journal of medical genetics.

A genetic study of Duchenne muscular dystrophy in West Midlands.

S. Bundey, 1981, Journal of medical genetics.

A genetic study of Duchenne muscular dystrophy in West Midlands.

S. Bundey, 1981, Journal of medical genetics.

Few psychological consequences of presymptomatic testing for Huntington disease

S. Bundey, 1997, The Lancet.

Chromosome Abnormalities and Genetic Counselling

D. Love, E. Whittle, S. Bundey, 1990 .