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Author/Creator MacDonald, F

2. Cryptic von Hippel-Lindau disease: germline mutations in patients with haemangioblastoma only. Issue 12 (1st December 2000)

Authors:
Hes, F J; McKee, S; Taphoorn, M J B; Rehal, P; van der Luijt, R B; McMahon, R; van der Smagt, J J; Dow, D; Zewald, R A; Whittaker, J; Lips, C J M; MacDonald, F; Pearson, P L; Maher, E R
Journal:
Journal of medical genetics
Issue:
Volume 37:Issue 12(2000)
Page Start:
939
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Epigenotype–phenotype correlations in Silver–Russell syndrome. Issue 11 (3rd August 2010)

Authors:
Wakeling, E L; Amero, S Abu; Alders, M; Bliek, J; Forsythe, E; Kumar, S; Lim, D H; MacDonald, F; Mackay, D J; Maher, E R; Moore, G E; Poole, R L; Price, S M; Tangeraas, T; Turner, C L S; Van Haelst, M M; Willoughby, C; Temple, I K; Cobben, J M
Journal:
Journal of medical genetics
Issue:
Volume 47:Issue 11(2010)
Page Start:
760
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗