Hypertrophic obstructive cardiomyopathy in a neonate with the carbohydrate-deficient glycoprotein syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800221
Reference5 articles.
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2. Harding BH, Dunger DB, Grant DB, Erdohazi M (1988) Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.J Neurol Neurosurg Psychiatr 51: 385–390.
3. Horslen SP, Clayton PT, Harding BN, Hall NA, Keir G, Winchester BG (1991) Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome.Arch Dis. Child 66: 1027–1032.
4. Jaeken J (1989) Disialotransferrin developmental deficiency and olivopontocerebellar atrophy.Arch Dis Child 64: 764–765.
5. Jaeken J, Stibler H, Hagberg B (1991) The carbohydrate-deficient glycoprotein syndrome.Acta Paediatr. Scand. Suppl. 375: [monograph].
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