1. Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria;Woo, S.L.; Lidskv, A.S.; Guttler, F.; Chandra, T.; Robson, J.H.;Nature,1983
2. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene;Monaco, A.; Neve, R.; Colletti-Feener, C.; Bertelson, C.; Kurnit, D.; Kunkel, L.;Nature,1986
3. Chromosome 5 allele loss in human colorectal carcinoma;Solomon, E.; Voss, R.; Hall, V.;Nature,1987
4. Evolution of sickle variant gene;Solomon, E.; Bodmer, W.F.;Lancet,1979
5. Highly variable minisatellites and DNA fingerprints;Jeffreys, A.J.;Biocm Soc Trans,1987