Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophy.

Author:

Jaeken J

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Disialotransferrin developmental deficiency syndrome;Kristiansson, B.; Andersson, M.; Tonnby, B.; Hagberg, B.;Arch Dis Child,1989

2. Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities;Harding, B.N.; Dunger, D.B.; Crant, D.B.; Erdohazi, M.;J Neurol Neurosurg Psychiatry,1988

3. An apparent homozygous X-linked disorder with carbohydrate-deficient serum glycoproteins;Jaeken, J.; Eggermont, E.; Stibler, H.;Lancet,1987

4. Micro anion exchange chromatography of carbohydrate-deficient transferrin in serum in relation to alcohol consumption;Stibler, H.; Borg, S.; Joustra, M.;Alcohol, Clinical and Experimental Research,1986

5. Clostridium difficile in an oncology unit;Brunetto, A.L.; Pearson, A.D.J.; Craft, A.W.; Pedler, S.J.;Arch Dis Child,1988

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