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Results 41-49 of 49 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1996Stable inheritance of an HLA-"blank" phenotype associated with a structural mutation in the HLA-A*0301 geneLienert, K.; Russ, G.; Lester, S.; Bennet, G.; Gao, X.; McCluskey, J.
1998Mild feline mucopolysaccharidosis type VI. Identification of an N-acetylgalactosamine-4-sulfatase mutation causing instability and increased specific activityYogalingam, G.; Hopwood, J.; Crawley, A.; Anson, D.
1998Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypesCrawley, A.; Yogalingam, G.; Muller, V.; Hopwood, J.
1998Genotype-phenotype correlations in mucopolysaccharidosis type I using enzyme kinetics, immunoquantification and in vitro turnover studiesBunge, S.; Clements, P.; Byers, S.; Kleijer, W.; Brooks, D.; Hopwood, J.
1998Somatic mutations, acetylator status, and prognosis in colorectal cancerHardingham, J.; Butler, W.; Roder, D.; Dobrovic, A.; Dymock, R.; Sage, R.; Roberts-Thomson, I.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
1999Evolution and molecular characterization of a β-globin gene from the Australian Echidna Tachyglossus aculeatus (Monotremata)Lee, M.H.; Shroff, R.; Cooper, S.; Hope, R.
1997The genome organisation of the Fanconi Anemia Group A (FAA) GeneIanzano, L.; d'Apolito, M.; Centra, M.; Savino, M.; Levran, O.; Auerbach, A.; Cleton-Jansen, A.M.; Doggett, N.; Pronk, J.; Tipping, A.; Gibson, R.; Mathew, C.; Whitmore, S.; Apostolou, S.; Callen, D.; Zelante, L.; Savoia, A.
1998Molecular genetics of mucopolysaccharidosis type I - mutation analysis among the patients of the former Soviet UnionVoskoboeva, E.; Krasnopolskaya, X.; Mirenburg, T.; Weber, B.; Hopwood, J.