Author:
Ramaekers V. T.,Stibler H.,Kint J.,Jaeken J.
Subject
Genetics(clinical),Genetics
Reference8 articles.
1. Wenner-Gren International Symposium Series;J. Jaeken,1989
2. Jaeken, J., Vanderschueren-Lodewyckx, M., Casaer, P.et al. Familial psychomotor retardation with markedly fluctuating serum prolactin, FSH and GH levels, partial TBG-deficiency, increased serum arylsulphatase A and increased CSF protein: a new syndrome?Pediatr. Res. 14 (1980) 179
3. Jaeken, J., van Eijk, H. G., van der Heul, C., Corbeel, L., Eeckels, R. and Eggermont, E. Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome.Clin. Chim. Acta 144 (1984) 245–247
4. Jaeken, J., Eggermont, E. and Stibler, H. An apparent homozygous X-linked disorder with carbohydrate-deficient serum glycoproteins.Lancet 2 (1987) 1398
5. Jaeken, J., Stibler, H., Kristiansson, B. and Blennow, G. Abstract,Vth International Congress Inborn Errors of Metabolism, Society for Inherited Metabolic Disorders, Pacific Grove, California, 1–5 June 1990
Cited by
63 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献