Search


Current filters:


Start a new search
Add filters:

Use filters to refine the search results.


Results 1-10 of 21 (Search time: 0.001 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
1996The human glycine receptor β subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genesHandford, C.; Lynch, J.; Baker, E.; Webb, G.; Ford, J.; Sutherland, G.; Schofield, P.
1996DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytesShibuya, A.; Campbell, D.; Hannum, C.; Yssel, H.; Franz-Bacon, K.; McClanahan, T.; Kitamura, T.; Nicholl, J.; Sutherland, G.; Lanier, L.; Phillips, J.
1996Identification of the gene FMR2, associated with FRAXE mental retardationGecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
1996Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21Wallace, R.; Berkovic, S.; Howell, R.; Sutherland, G.; Mulley, J.
1996Characterization and chromosomal localization of the human A2a adenosine receptor gene - ADORA2ALe, F.; Townsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1996Assignment of the Gene For Beta-Casein (CSN2) to 4q13-q21 in Humans and 3p13-p12 in ChimpanzeesMcConkey, E.; Menon, R.; Williams, G.; Baker, E.; Sutherland, G.
1996Dynamic mutation loci: Allele distributions in different populationsRichards, R.; Crawford, J.; Narahara, K.; Mangelsdorf, M.; Friend, K.; Staples, A.; Denton, M.; Easteal, S.; Hori, T.; Kondo, I.; Jenkins, T.; Goldman, A.; Panich, V.; Ferakova, E.; Sutherland, G.
1996Fragile X Syndrome and other X-linked Causes of Mental HandicapSutherland, G.; Mulley, J.
1996FRAGILE X SYNDROME AND FRAGILE XE MENTAL RETARDATION [Review]Sutherland, G.; Mulley, J.
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.