Population studies of the fragile X: a molecular approach.

Author:

Jacobs P A,Bullman H,Macpherson J,Youings S,Rooney V,Watson A,Dennis N R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Preventive screening for the fragile X syndrome;Turner, G.; Robinson, H.; Laing, S.; Purvis-Smith, S.;N Engl 7 Med,1986

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

3. Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats, FRAXACI and FRAXAC2, which immediately flank the fragile site;Richards, R.I.; Holman, K.; Kozman, H.;J Med Genet,1991

4. Evidence of founder chromosomes in fragile-X syndrome;Richards, R.I.; Holman, K.; Friend, K.;Nature Genet,1992

5. Population screening for fragile-X;Turner, G.; Robinson, H.; Laing, S.;Lancet,1992

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