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Author/Creator Hol, F A

2. A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy. Issue 3 (22nd October 2007)

Authors:
Jonckheere, A I; Hogeveen, M; Nijtmans, L G J; van den Brand, M A M; Janssen, A J M; Diepstra, J H S; van den Brandt, F C A; van den Heuvel, L P; Hol, F A; Hofste, T G J; Kapusta, L; Dillmann, U; Shamdeen, M G; Smeitink, J A M; Rodenburg, R J T
Journal:
Journal of medical genetics
Issue:
Volume 45:Issue 3(2008)
Page Start:
129
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3. Issue 9 (1st September 2004)

Authors:
Solomon, N M; Ross, S A; Morgan, T; Belsky, J L; Hol, F A; Karnes, P S; Hopwood, N J; Myers, S E; Tan, A S; Warne, G L; Forrest, S M; Thomas, P Q
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 9(2004)
Page Start:
669
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗