K. Kelly

发表

Ascertainment of myotonic dystrophy through cataract by selective screening.

N. Haites, P. Turnpenny, J. Dean, 1995, Journal of medical genetics.

Intelligence quotient profile in myotonic dystrophy, intergenerational deficit, and correlation with CTG amplification.

P. Turnpenny, K. Kelly, C. Clark, 1994, Journal of medical genetics.

Autosomal dominant retinitis pigmentosa (ADRP): a rhodopsin mutation in a Scottish family.

Carolyn A. Converse, N. Haites, L. Esakowitz, 1992, Journal of medical genetics.

Linkage studies with 17q and 18q markers in a breast/ovarian cancer family.

H. Kitchener, D. Cruickshank, N. Haites, 1993, American journal of human genetics.

Antenatal screening for carriers of cystic fibrosis: randomised trial of stepwise v couple screening

T. Marteau, Z. Miedzybrodzka, N. Haites, 1995, BMJ.

Early loss of heterozygosity on 17q in ovarian cancer. The Abe Ovarian Cancer Genetics Group.

D. Eccles, D. Bell, N. Haites, 1992, Oncogene.

No Excess of Factor V:Q506 Genotype but High Prevalence of Anticardiolipin Antibodies without Antiendothelial Cell Antibodies in Retinal Vein Occlusion in Young Patients

M. Davidson, J. Currie, M. Greaves, 2001, Ophthalmologica.

Haemochromatosis mutations in North‐East Scotland

Z. Miedzybrodzka, N. Haites, M. Pippard, 1999, British journal of haematology.

Evaluation of laboratory methods for cystic fibrosis carrier screening: reliability, sensitivity, specificity, and costs.

Z. Miedzybrodzka, N. Haites, K. Kelly, 1994, Journal of medical genetics.

Prenatal diagnosis for the cystic fibrosis mutation 1717‐1, G→A using arms

Z. Miedzybrodzka, N. Haites, S. Little, 1992, Prenatal diagnosis.

sensitivity , specificity , and costs . fibrosis carrier screening : reliability , Evaluation of laboratory methods for cystic

Z. Miedzybrodzka, N. Haites, K. Kelly, 2022 .

Thrombosis, markers of thrombotic risk, indwelling central venous catheters and antithrombotic prophylaxis using low-dose warfarin in subjects with malignant disease.

M. Davidson, M. Greaves, K. Kelly, 1999, Clinical and laboratory haematology.

Rapid diagnosis and identification of cross-over sites in patients with glucocorticoid remediable aldosteronism.

J. Connell, N. Haites, A. Macconnachie, 1998, The Journal of clinical endocrinology and metabolism.

Antenatal cystic fibrosis carrier screening--whether, when and how?

T. Marteau, Z. Miedzybrodzka, N. Haites, 1993, Paediatric and perinatal epidemiology.

Prevalence of cystic fibrosis mutations in the Grampian region of Scotland.

Z. Miedzybrodzka, N. Haites, J. Dean, 1993, Journal of medical genetics.

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

M. Ferguson-Smith, I. Hausmanowa-Petrusewicz, J. Yates, 1986, Journal of medical genetics.

p53 mutation is a common genetic event in ovarian carcinoma.

H. Kitchener, D. Eccles, N. Haites, 1993, Cancer research.

Start a DNA diagnostic service.

N. Haites, K. Kelly, A. Johnston, 1988, BMJ.

Repeated freezing and thawing of peripheral blood and DNA in suspension: effects on DNA yield and integrity.

N. Haites, K. Kelly, K S Ross, 1990, Journal of medical genetics.

Linkage in a family with X‐linked Charcot‐Marie‐Tooth disease

N. Haites, K. Kelly, C. Clark, 1989, Clinical genetics.

The diagnosis of myotonic dystrophy.

P. Turnpenny, K. Kelly, 1993, Scottish medical journal.

The influence of birth weight and genetic factors on lipid levels: a study in adult twins

P. Haggarty, G. Mcneill, D. Campbell, 2006, British Journal of Nutrition.

Fragile X syndrome with FMR1 and FMR2 deletion

Z. Miedzybrodzka, J. Dean, K. Kelly, 1999, Journal of medical genetics.

A general method for the detection of large CAG repeat expansions by fluorescent PCR.

D. Goudie, D. Fitzpatrick, D J Brock, 1996, Journal of medical genetics.

Screening for carriers of cystic fibrosis.

Z. Miedzybrodzka, J. Dean, A. Shrimpton, 1991, BMJ.

Ascertainment ofmyotonic dystrophy through cataractbyselective screening

N. Haites, A. Kidd, K. Kelly, 2011 .

The influence of birth weight and genetic factors on lipid levels: a study in adult twins

P. Haggarty, G. Mcneill, D. Campbell, 2006, British Journal of Nutrition.