First trimester diagnosis of Inherited Metabolic Disease: Experience in the UK
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800583
Reference5 articles.
1. Fowler, B., Giles, L., Sardharwalla, I. B. and Clayton, J. K. First trimester diagnosis of methylmalonic acidura.Prenatal Diagnosis 8 (1988) 207–213
2. Galjaard, H. Biochemical analysis of chorionic villi: a worldwide survey of first trimester fetal diagnosis of inborn errors of metabolism. In: Fraccaro, M., Simoni, G. and Brambati, B. (eds.),First Trimester Diagnosis, Springer-Verlag, Berlin, 1985, pp. 209–217
3. Poenaru, L. First trimester diagnosis of metabolic diseases: A survey in countries from the European Community.Prenatal Diagnosis 7 (1987) 333–341
4. Sanguinetti, N., Marsh, J., Jackson, M., Fensom, A. H., Warren, R. C. and Rodeck, C. H. The arylsulphatases of chorionic villi: potential problems in the first trimester diagnosis of metachromatic leucodystrophy and Maroteaux-Lamy disease.Clin. Genet. 30 (1986) 302–308
5. Vimal, C. M., Fensom, A. H., Heaton, D., Ward, R. H. T., Garrod, P. and Penketh, R. J. A. Prenatal diagnosis of argininosuccinicaciduria by analysis of cultured chorionic villi.Lancet 2 (1984) 521–522
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