Genetic counselling and the work of a medical genetics centre

A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.

Journal of medical genetics·1992

A recombinant-based feline immunodeficiency virus antibody enzyme-linked immunosorbent assay.

Veterinary immunology and immunopathology·1992

A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling.

Journal of medical genetics·1992

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. II. Invasive epithelial ovarian cancers in white women. Collaborative Ovarian Cancer Group.

American journal of epidemiology·1992

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. I. Methods. Collaborative Ovarian Cancer Group.

American journal of epidemiology·1992

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. IV. The pathogenesis of epithelial ovarian cancer. Collaborative Ovarian Cancer Group.

American journal of epidemiology·1992

Health promotion in the general practice setting.

Health visitor·1995

Developing an immunisation protocol for the primary health care team.

Health visitor·1995

Working together for the care of elderly people.

Health visitor·1995

Ethnic minorities. The role of health advocates in health visiting teams.

Health visitor·1995

Supporting vulnerable families: an evaluation of Newpin.

Health visitor·1995

Parenting. Working with young men.

Health visitor·1995

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

iScience·2026

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Journal of equine science·2026

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Frontiers in medicine·2026

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

EBioMedicine·2026

Cross-Ethnic Replication of Intersectin-1 as a Parkinson's Disease Susceptibility Gene in a Large Chinese Cohort.

Movement disorders : official journal of the Movement Disorder Society·2026

Chromosomal abnormalities in isolated persistent left superior vena cava: A systematic review and meta-analysis.

Turkish journal of obstetrics and gynecology·2026

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A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.

A recombinant-based feline immunodeficiency virus antibody enzyme-linked immunosorbent assay.

A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling.

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. II. Invasive epithelial ovarian cancers in white women. Collaborative Ovarian Cancer Group.

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. I. Methods. Collaborative Ovarian Cancer Group.

Characteristics relating to ovarian cancer risk: collaborative analysis of 12 US case-control studies. IV. The pathogenesis of epithelial ovarian cancer. Collaborative Ovarian Cancer Group.

Health promotion in the general practice setting.

Developing an immunisation protocol for the primary health care team.

Working together for the care of elderly people.

Ethnic minorities. The role of health advocates in health visiting teams.

Supporting vulnerable families: an evaluation of Newpin.

Parenting. Working with young men.

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

Cross-Ethnic Replication of Intersectin-1 as a Parkinson's Disease Susceptibility Gene in a Large Chinese Cohort.

Chromosomal abnormalities in isolated persistent left superior vena cava: A systematic review and meta-analysis.

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Genetic counselling and the work of a medical genetics centre

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