Molecular genetics as a 'probe' in ophthalmology.

Por Haites, N
Publicado em 1993

Genetic aspects of Charcot-Marie-Tooth disease

Por BELL, C., HAITES, N.
Publicado em 1998

Royal Society discussion meeting: Prevention and Avoidance of Genetic Disease, held on 29 to 30 April 1987 at the Royal Society.

Por Haites, N, Johnston, A W
Publicado em 1988

A new approach to prenatal cystic fibrosis carrier screening.

Por Miedzybrodzka, Z, Haites, N, Dean, J
Publicado em 1993

Genetic prediction of adult onset disease.

Por Simpson, S. A., Dean, J. C., Haites, N.
Publicado em 1994

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

Por Ross, K S, Haites, N E, Kelly, K F
Publicado em 1990

Sequential occurrence within three years in a premenopausal woman of cervical, ovarian, and endometrial cancers

Por Cumming, G, Narayansingh, G, Parkin, D, Haites, N
Publicado em 2001

Method of assessing the reproducibility of blood flow measurement: factors influencing the performance of thermodilution cardiac output computers.

Por Mackenzie, J D, Haites, N E, Rawles, J M
Publicado em 1986

One thousand heart attacks in Grampian: the place of cardiopulmonary resuscitation in general practice.

Por Pai, G R, Haites, N E, Rawles, J M
Publicado em 1987

Start a DNA diagnostic service.

Por Kelly, K. F., Haites, N. E., Johnston, A. W.
Publicado em 1988

Partial trisomy 7 (q32----qter) syndrome in two children.

Por Couzin, D A, Haites, N, Watt, J L, Johnston, A W
Publicado em 1986

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

Por Miedzybrodzka, Z H, Yin, Z, Kelly, K F, Haites, N E
Publicado em 1994

Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation

Por Donaghy, M, Sisodiya, S, Kennett, R, McDonald, B, Haites, N, Bell, C
Publicado em 2000

Assessment of cardiac output by the Doppler ultrasound technique alone.

Por Haites, N E, McLennan, F M, Mowat, D H, Rawles, J M
Publicado em 1985

Rhodopsin mutations in a Scottish retinitis pigmentosa population, including a novel splice site mutation in intron four.

Por Bell, C, Converse, C A, Hammer, H M, Osborne, A, Haites, N E
Publicado em 1994

Identification of women at high genetic risk of breast cancer through the National Health Service Breast Screening Programme (NHSBSP).

Por de Silva, D, Gilbert, F, Needham, G, Deans, H, Turnpenny, P, Haites, N
Publicado em 1995

Impairment of colour vision in workers exposed to organic solvents

Por Semple, S, Dick, F, Osborne, A, Cherrie, J, Soutar, A, Seaton, A, Haites, N
Publicado em 2000

p53 mutation and expression in lymphoma.

Por Adamson, D. J., Thompson, W. D., Dawson, A. A., Bennett, B., Haites, N. E.
Publicado em 1995

Ascertainment of familial ovarian cancer in the Aberdeen Genetic Clinic.

Por Gregory, H, Schofield, A, de Silva, D, Semper, J, Milner, B, Allan, L, Haites, N
Publicado em 1996

Variation of phenotype in patients with glucocorticoid remediable aldosteronism.

Por Gates, L J, MacConnachie, A A, Lifton, R P, Haites, N E, Benjamin, N
Publicado em 1996