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Now showing items 1-6 of 6

Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta

Le Blanc, Katarina; Götherström, Cecilia; Ringdén, Olle; Hassan, Moustapha; McMahon, Robert; Horwitz, Edwin; Anneren, Göran; Axelsson, Ove; Nunn, Janice; Ewald, Uwe; Nordén-Lindeberg, Solveig; Jansson, Monika; Dalton, Ann; Aström, Eva; Westgren, Magnus (2005-06-15)
Cryptic von Hippel-Lindau disease : germline mutations in patients with haemangioblastoma only

Hes, F. J.; McKee, S.; Taphoorn, M. J.; Rehal, P.; van Der Luijt, R. B.; McMahon, R; van Der Smagt, J. J.; Dow, D.; Zewald, R. A.; Whittaker, J.; Lips, C. J.; MacDonald, F.; Pearson, P. L.; Maher, E. R. (2000-12)
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families

McMahon, R; Mulligan, L M; Healey, C S; Payne, S J; Ponder, M; Ferguson-Smith, M A; Barton, D E; Ponder, B A (1994-04)
Cystic fibrosis transmembrane conductance regulator gene mutations in severe nasal polyposis

Irving, R M; McMahon, R; Clark, R; Jones, N S (1997-12)
Genotype analysis in cystic fibrosis in relation to the occurrence of diabetes mellitus

Hamdi, I.; Payne, S. J.; Barton, D. E.; McMahon, R.; Green, M.; Shneerson, J. M.; Hales, C. N. (1993-04)
Cystic fibrosis identified by neonatal screening : incidence, genotype, and early natural history

Green, M R; Weaver, L T; Heeley, A F; Nicholson, K; Kuzemko, J A; Barton, D E; McMahon, R; Payne, S J; Austin, S; Yates, J R (1993-04)

Now showing items 1-6 of 6