S. Holloway

发表

Long-Term Attendance at Follow-Up of Women Assessed as Being at Increased Risk of Developing Breast Cancer in South-East Scotland

H. Campbell, M. Porteous, R. Cetnarskyj, 2007, Public Health Genomics.

Uptake of testing for BRCA1/2 mutations in South East Scotland

H. Campbell, B. Bernhard, S. Holloway, 2008, European Journal of Human Genetics.

Linkage disequilibrium and recombination make a telomeric site for the Huntington's disease gene unlikely.

R. Snell, A. Curtis, A. Shrimpton, 1991, Journal of medical genetics.

Patient satisfaction with two different models of cancer genetic services in south-east Scotland

H. Campbell, M. Porteous, R. Cetnarskyj, 2004, British Journal of Cancer.

Motor neurone disease in the Lothian Region of Scotland 1961-81.

J. Mitchell, S. Holloway, 1986, Journal of epidemiology and community health.

International collaborative study of the spinal muscular atrophies Part 2. Analysis of genetic data

A. Davie, A. Emery, S. Holloway, 1976, Journal of the Neurological Sciences.

PREDICTIVE TESTING FOR HUNTINGTON'S DISEASE WITH LINKED DNA MARKERS

A. Curtis, L. Barron, J. Raeburn, 1989, The Lancet.

Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades?

J. Tolmie, S. Holden, R. McGowan, 2013, Clinical genetics.

Referrals of patients to colorectal cancer genetics services in south-east Scotland

H. Campbell, M. Porteous, R. Cetnarskyj, 2004, Familial Cancer.

International collaborative study of the spinal muscular atrophies Part 1. Analysis of clinical and laboratory data

A. Davie, I. Hausmanowa-Petrusewicz, A. Emery, 1976, Journal of the Neurological Sciences.

Further evidence of the increased risk for malignant peripheral nerve sheath tumour from a Scottish cohort of patients with neurofibromatosis type 1

W. Lam, S. Holloway, R. Davidson, 2007, Journal of Medical Genetics.

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.

M. Porteous, D. Brock, L. Barron, 1993, Journal of medical genetics.

First‐trimester maternal serum biochemical indicators in Down syndrome

D. Brock, L. Barron, M. Seppala, 1990, Prenatal diagnosis.

Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis

A. Curtis, D. Brock, L. Strain, 1988, Human Genetics.

What do young people think about screening for cystic fibrosis?

R. Elton, J. Raeburn, S. Holloway, 1991, Journal of medical genetics.

Prenatal exclusion testing for Huntington's disease: a problem of too much information.

A. Curtis, M. Boxer, D. Brock, 1989, Journal of medical genetics.

An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance.

C. Hayward, D. Brock, J. Livingstone, 1992, American journal of human genetics.

1961-81 . Lothian Region of Scotland Motor neurone disease in the

J. Mitchell, S. Holloway, 2022 .

The Scottish Motor Neuron Disease Register: a prospective study of adult onset motor neuron disease in Scotland. Methodology, demography and clinical features of incident cases in 1989.

P. Sandercock, B. Pentland, C. Warlow, 1992, Journal of neurology, neurosurgery, and psychiatry.

Predicting breast cancer risk: implications of a “weak” family history

M. Longmuir, D. Goudie, N. Bradshaw, 2008, Familial Cancer.

Prospective surveillance of women with a family history of breast cancer: auditing the risk threshold

M. Longmuir, D. Goudie, N. Bradshaw, 2008, British Journal of Cancer.

Risks of fetal cystic fibrosis based on linkage disequilibrium data

D. Brock, S. Holloway, 1989, Human Genetics.

Cascade Testing for the Identification of Carriers of Cystic Fibrosis

S. Holloway, D. Brock, 1994, Journal of medical screening.

First‐trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes

G. Besley, A. Curtis, J. Raeburn, 1988, Prenatal diagnosis.

Colonoscopy surveillance of individuals at risk of familial colorectal cancer

N. Bradshaw, M. Porteous, M. Dunlop, 2003, Gut.

Life expectancy and death from cardiomyopathy amongst carriers of Duchenne and Becker muscular dystrophy in Scotland

D. Goudie, M. Porteous, M. Denvir, 2007, Heart.

Changes in maternal age distribution and their possible impact on demand for prenatal diagnostic services

D. Brock, S. Holloway, 1988, British medical journal.

Fertility of older women

D. Brock, S. Holloway, 1990, The Lancet.

A randomised controlled trial of breast cancer genetics services in South East Scotland: psychological impact

H. Campbell, H. Campbell, M. Porteous, 2003, British Journal of Cancer.

Predictive testing for Huntington disease: social characteristics and knowledge of applicants, attitudes to the test procedure and decisions made after testing

A. Wright, D. Brock, L. Barron, 1994, Clinical genetics.

The epidemiology of motor neuron disease in Scotland

A. Emery, A. Emery, S. Holloway, 1982, Muscle & nerve.

Motor neurone disease intheLothian Region Scotland 1961-81 of

S. Holloway, JD Mitchell, 1986 .

Referrals of women with a family history of breast cancer from primary care to cancer genetics services in South East Scotland

H. Campbell, M. Porteous, R. Cetnarskyj, 2003, British Journal of Cancer.

The prognosis of adult-onset motor neuron disease: a prospective study based on the Scottish Motor Neuron Disease Register

J. Slattery, C. Warlow, R. Swingler, 1993, Journal of Neurology.

Genetic linkage between Huntington's disease and D4S10(G8) in Scottish families

A. Curtis, S. Holloway, D. Brock, 1989, Clinical genetics.

Presymptomatic testing for Huntington's disease

A. Curtis, D. Brock, J. Raeburn, 2004, Human Genetics.

Inequality of use of Cancer Genetics Services by members of breast, ovarian and colorectal cancer families in South East Scotland

H. Campbell, R. Cetnarskyj, B. Bernhard, 2008, Familial Cancer.

DNA TYPING TO AVOID NEED FOR PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

J. Burn, A. Curtis, R. Nelson, 1986, The Lancet.

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

P. Brennan, J. Burn, J. Deanfield, 1998, The Lancet.