Genetic counselling
37 results
1 - 37Genetic counselling
Genetic testing
Thalassaemias
Interventions to improve psychosocial well‐being in female BRCA‐mutation carriers following risk‐reducing surgery
Sickle cell anaemia
Hereditary susceptibility to cancer
Hereditary myopathies
Screening for fetal chromosomal abnormalities
Retinoblastoma
Dilated cardiomyopathy
Cancer genetic risk assessment for individuals at risk of familial breast cancer
Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay‐Sachs disease
Klinefelter’s syndrome
Rare diseases
Preconception and antenatal screening for the fragile site on the X‐chromosome
Antenatal clinics and specialist care: consultations, referrals, treatment guidelines
Amyotrophic lateral sclerosis (ALS)
Diabetes: definition, differential diagnosis and classification
Turner syndrome
Common antiepileptic drugs in pregnancy in women with epilepsy: Cochrane systematic review
Interventions for promoting physical activity in people with cystic fibrosis
Screening for reducing morbidity and mortality in malignant melanoma
Nutrition‐specific interventions for preventing and controlling anaemia throughout the life cycle: an overview of systematic reviews
Risk‐reducing mastectomy for the prevention of primary breast cancer
Ventricular tachycardia
Polycystic kidney disease