Origins of the fragile X syndrome mutation.

Author:

Hirst M C,Knight S J,Christodoulou Z,Grewal P K,Fryns J P,Davies K E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium;Sutherland, G.R.;Science,1977

2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in the fragile X syndrome;Verkerk, A.J.M.H.; Sutcliffe, Pieretti M.; J.S.;Cell,1991

3. Fragile X genotype characterised by an unstable region of DNA;Yu, S.; Pritchard, M.; Kremer, E.;Science,1991

4. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n;Kremer, E.J.; Pritchard, M.; Lynch, M.;Science,1991

5. Molecular heterogeneity of the fragile X syndrome;Nakahori, Y.; Knight, S.J.L.; Holland, J.;Nucleic Acids Res,1991

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