Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation.

Author:

Rousseau F,Heitz D,Oberle I,Mandel J L

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. Abnormal pattern detected in fragile-X patients by pulsedfield gel electrophoresis;Vincent, A.; Heitz, D.; Petit, C.; Kretz, C.; Oberle, I.; Mandel, J.-L.;Nature,1991

2. Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island;Heitz, D.; Rousseau, F.; Devys, D.;Science,1991

3. Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome;Bell, M.V.; Hirst, M.C.; Nakahori, Y.;Cell,1991

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

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

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