Author/Creator: Hoffmann, G F - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Hoffmann, G F

1. A novel mutation (c.64_65delGGinsAACC [p.G21fsX66]) in the GTP cyclohydrolase 1 gene that causes Segawa disease. Issue 2 (17th January 2008)

Authors:: von Mering, M; Gabriel, H; Opladen, T; Hoffmann, G F; Storch, A
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 79:Issue 2(2008)
Page Start:: 229
Record Type:: Journal Article
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2. Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblasts. Issue 5 (19th January 2007)

Authors:: Haas, D; Morgenthaler, J; Lacbawan, F; Long, B; Runz, H; Garbade, S F; Zschocke, J; Kelley, R I; Okun, J G; Hoffmann, G F; Muenke, M
Journal:: Journal of medical genetics
Issue:: Volume 44:Issue 5(2007)
Page Start:: 298
Record Type:: Journal Article
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3. Nature and nurture in vitamin B12 deficiency. Issue 1 (1st July 2002)

Authors:: Zschocke, J; Schindler, S; Hoffmann, G F; Albani, M
Journal:: Archives of disease in childhood
Issue:: Volume 87:Issue 1(2002)
Page Start:: 75
Record Type:: Journal Article
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4. Pyridoxal phosphate-dependent neonatal epileptic encephalopathy. Issue 2 (22nd February 2008)

Authors:: Bagci, S; Zschocke, J; Hoffmann, G F; Bast, T; Klepper, J; Müller, A; Heep, A; Bartmann, P; Franz, A R
Journal:: Archives of disease in childhood
Issue:: Volume 93:Issue 2(2008)
Page Start:: F151
Record Type:: Journal Article
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