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Results 1-10 of 83 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
1995Fragile X syndrome and other dynamic mutation diseasesSutherland, G.; Richards, R.
1996FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]Sutherland, G.; Mulley, J.
1999Gamma-Heregulin: a fusion gene of DOC-4 and neuregulin-1 derived from a chromosome translocationLiu, X.; Baker, E.; Eyre, H.; Sutherland, G.; Zhou, M.
1996Positional cloning of the Fanconi anaemia group A geneApostolou, S.; Whitmore, S.; Crawford, J.; Lennon, G.; Sutherland, G.; Callen, D.; Ianzano, L.; Savino, M.; d'Apolito, M.; Notarangelo, A.; Memeo, E.; Piemontese, M.; Zelante, L.; Savoia, A.; Gibson, R.; Tipping, A.; Morgan, N.; Hassock, S.; Jansen, S.; de Ravel, T.; et al.
1995Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to 20q13.2Phillips, H.; Scheffer, I.; Berkovic, S.; Hollway, G.; Sutherland, G.; Mulley, J.
1995Bovine latent transforming growth factor β1-binding protein 2: molecular cloning, identification of tissue isoforms, and immunolocalization to elastin-associated microfibrilsGibson, M.; Hatzinikolas, G.; Davis, E.; Baker, E.; Sutherland, G.; Mecham, R.
1998Molecular characterization, pharmacological properties and chromosomal localization of the human GALR2 galanin receptorFathi, Z.; Battaglino, P.; Iben, L.; Li, H.; Baker, E.; Zhang, D.; McGovern, R.; Mahle, C.; Sutherland, G.; Iismaa, T.; Dickinson, K.; Antal Zimanyi, I.
1998Fragile sites still breaking [Review]Sutherland, G.; Baker, E.; Richards, R.
1995Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeScott, H.; Blanch, L.; Guo, X.; Freeman, C.; Orsborn, A.; Baker, E.; Sutherland, G.; Morris, C.; Hopwood, J.
1995An integrated physical map of human chromosome 16Doggett, N.; Goodwin, L.; Tesmer, J.; Meincke, L.; Bruce, D.; Clark, L.; Altherr, M.; Ford, A.; Chi, H.; Marrone, B.; Longmire, J.; Lane, S.; Whitmore, S.; Lowenstein, N.; Sutherland, G.; Mundt, M.; Knill, E.; Bruno, W.; Macken, C.; Torney, D.; et al.