Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Author:

Richards R I,Holman K,Kozman H,Kremer E,Lynch M,Pritchard M,Yu S,Mulley J,Sutherland G R

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Genetic mapping of new RFLPs at Xq27-q28;Suthers, G.K.; Oberle, I.; Nancarrow, J.,1991

2. Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome;Suthers, G.K.; Mulley, J.C.; Voelckel, M.A.;Am J Hum Genet,1991

3. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction;Weber, J.L.; May, P.E.;Am J Hum Genet,1989

4. Fragile X linked mental retardation: diagnosis using highly polymorphic microsatellite markers;Richards, R.I.; Shen, Y.; Holnan, K.;Am J Hum Genet,1991

5. Isolation of a human DNA sequence which spans the fragile X;Kremer, E.J.; Yu, S.; Pritchard, M.;Am J Hum Genet

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