Prenatal exclusion testing for Huntington's disease: a problem of too much information.

Author:

Millan F A,Curtis A,Mennie M,Holloway S,Boxer M,Faed M J,Crawford J W,Liston W A,Brock D J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. The prevention of Huntington's chorea;Harper, P.S.;J R Coll Physicians Lond,1986

2. Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA marker;Quarrell, O.W.J.; Meredith, A.L.; Tyler, A.;Lancet,1987

3. First-trimester prenatal diagnosis for Huntington's disease with DNA probes;Hayden, M.R.; Hewitt, J.; Kastelein, J.J.P.;Lancet,1987

4. A DNA segment encoding two genes very tightly linked to Huntington's disease;Gilliam, T.C.; Bucan, M.; MacDonald, M.E.;Science,1987

5. Interpretation of the properties of chromatin extracts from mammalian nuclei;Marshall, A.J.; Burgoyne, L.A.;Nucleic Acids Res,1976

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1. Genetic counseling and testing for Huntington's disease: A historical review;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2016-05-13

2. Inherited Diseases;Tietz Textbook of Clinical Chemistry and Molecular Diagnostics;2012

3. Negotiating Responsibility: Case Studies of Reproductive Decision-Making and Prenatal Genetic Testing in Families Facing Huntington Disease;Journal of Genetic Counseling;2005-06

4. Huntington's disease;Prenatal Diagnosis;1996-12

5. Genetic tests: evolving policy questions;IEEE Technology and Society Magazine;1996

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