1. A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome;Jacobs, P.A.; Betts, P.R.; Cockwell, A.E.;Ann Hum Genet,1990
2. A gene from the region of the human X-inactivation centre is expressed exclusively from the inactive X-chromosome;Brown, C.J.; Ballabio, A.; Rupert, J.L.;Nature,1991
3. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms;Clemens, P.R.; Fenwick, R.G.; Chamberlain, J.S.;Am J Hum Genet,1991
4. Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene;Feener, C.A.; Boyce, F.M.; Kunkel, L.M.;Am J Hum Genet,1991
5. Turner syndrome patients with a ring X chromosome;Berkovitz, G.; Stamberg, J.; Plotnick, L.P.; Lanes, R.;Clin Genet,1983