UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders.

Author:

Firth H V,Lindenbaum R H

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Identification of the cystic fibrosis gene: cloning and characterisation of complementary DNA;Riordan, JR, Rommens; JM, Kerem; B.;Science,1989

2. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffnan, E.P.; Brown, R.H.; Kunkel, L.M.;Cell,1987

3. First-trimester fetal diagnosis for the haemoglobinopathies: three cases;Old, J.M.; Ward, R.H.T.; Petrou, M.;Lancet,1982

4. Demand for DNA probe testing in three genetic centres in Britain;Rona, R.; Swan, A.; Beech, R.;J Med Genet,1987

5. Prenatal diagnosis for the detection of Down syndrome: why are so few eligible women tested?;Lippman-Hand, A.; Piper, M.;Prenat Diagn,1981

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