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Results 1-10 of 12 (Search time: 0.009 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Fragile sites still breaking [Review]Sutherland, G.; Baker, E.; Richards, R.
1995Fragile X syndrome and other dynamic mutation diseasesSutherland, G.; Richards, R.
1998FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesisHewett, D.; Handt, O.; Hobson, L.; Mangelsdorf, M.; Eyre, H.; Baker, E.; Sutherland, G.; Schuffenhauer, S.; Mao, J.; Richards, R.
1995The molecular basis of fragile sites in human chromosomesSutherland, G.; Richards, R.
1997Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatYu, S.; Mangelsdorf, M.; Hewett, D.; Hobson, L.; Baker, E.; Eyre, H.; Lapsys, N.; Le Paslier, D.; Doggett, N.; Sutherland, G.; Richards, R.
1999Human Genetics '99: Trinucleotide Repeats Fragile Sites-Cytogenetic Similarity with Molecular DiversitySutherland, G.; Richards, R.
1995Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locusNancarrow, J.; Holman, K.; Hori, T.; Denton, M.; Sutherland, G.; Richards, R.
1996REPEAT OFFENDERS - SIMPLE REPEAT SEQUENCES AND COMPLEX GENETIC PROBLEMS [Review]Richards, R.; Sutherland, G.
1997Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal diseaseNarahara, K.; Baker, E.; Ito, S.; Yokoyama, Y.; Yu, S.; Hewitt, D.; Sutherland, G.; Eccles, M.; Richards, R.
1995Simple tandem DNA repeats and human genetic diseaseSutherland, G.; Richards, R.