The Genetic Testing of Children

Guidelines for the molecular genetics predictive test in Huntington's disease. J Med Genet 1994; 31: 555–9

The genetic testing of children. Report of a working party of the Clinical Genetics Society (UK). J Med Genet 1994; 31: 785–7

Binedell J , Soldan JR , Scourfield J , Harper PS . Huntington's disease predictive testing: the case for an assessment approach to requests from adolescents. J Med Genet 1996; 33: 912–18.

Kessler S. Invited essay on the psychological aspects of genetic counselling. V. Preselection: a family coping strategy in Huntington disease. Am J Med Genet 1988; 31: 617–21.

Marteau TM , van Duijn M , Ellis I. Effects of genetic screening on perceptions of health: a pilot study. J Med Genet 1992; 29: 24–6.

Goodall J. Helping a child to understand her own testicular feminisation. Lancet 1991; 337: 33–5.

Burn J. Familial adenomatous polyposis. Arch Dis Child 1994; 71: 103–7.

Wray R , Neil HAW , Rees JAE . Screening for hyperlipidaemia in childhood. J R Coll Vhys Land 1996; 30: 115–18.

Geva T , Hegesh J , Frand M. The clinical course and echocardiography features of Marfan's syndrome in childhood. Am J Dis Child 1987; 141: 1179–82.

Shores J , Berger KR , Murphy EA , Pyeritz RE . Progression of aortic dilatation and the benefit of long-term beta-adrenergic blockade in Marfan's syndrome. N Engl J Med 1994; 330: 1335–41.

Ravine D , Walker RG , Gibson RN , Sheffield LJ , Kincaid-Smith P , Danks DM . Treatable complications in undiagnosed cases of autosomal dominant polycystic kidney disease. Lancet 1991; 337: 127–9.

Evans DGR , Huson SM , Donnai D. A genetic study of neurofibromatosis type 2 in the United Kingdom. Guidelines for genetic counselling. J Med Genet 1992; 29: 847–52.

Maddock IR , Moran A , Maher ER . A genetic register for von Hippel-Lindau disease. J Med Genet 1996; 33: 120–7.

Morrison PJ , Hadden DR , Russell CFJ , Hughes AE , Powell D , Nevin NC . A protocol for testing for MEN2A gene carriers in childhood. J Med Genet 1996; 33: Suppl 1; SP17

Wertz DC , Fanos JH , Reilly PR . Genetic testing for children and adolescents. JAMA 1994; 272: 875–81.

Genetic testing for familial hypertrophic cardiomyopathy in newborn infants. BMJ 1995; 310: 856–9

Goodwin JF . Hypertrophic cardiomyopathy can be treated but not cured. BMJ 1995; 311: 58

Marteau T , Michie S. A positive screening test for an untreatable condition provided psychological relief from uncertainty. BMJ 1995; 311: 58–9.

Dalby S. GIG response to the UK Clinical Genetics Society report “The Genetic Testing of Children”. J Med Genet 1995; 32: 490–4.

Balfour-Lynn I , Madge S , Dinwiddie R. Testing carrier status in siblings of patients with cystic fibrosis. Arch Dis Child 1995; 72: 167–8.

Barnes C. Genetic testing of children. Fourth European Conference of Psychosocial Aspects of Genetics, Heidelberg, 1994.

Laird L , Dezateux C , Anionwu EN . Neonatal screening for sickle cell disorders: what about the carrier infants? BMJ 1996; 313: 407–11.

Marteau T. The genetic testing of children. J Med Genet 1994; 31: 743