Author:
Matalon R.,Michals K.,Azen C.,Friedman E. G.,Koch R.,Wenz E.,Levy H.,Rohr F.,Rouse B.,Castiglioni L.,Hanley W.,Austin V.,de la Cruz F.
Subject
Genetics(clinical),Genetics
Reference5 articles.
1. Dent, C. E. Relation of biochemical abnormality to development of mental defect in phenylketonuria.Report of 23rd Ross Pediatric Research Conference, Ross Laboratories, Columbus, Ohio, 1957, p. 32
2. Lenke, R. R. and Levy, H. L. Maternal phenylketonuria and hyperphenylalaninemia.N. Engl. J. Med. 303 (1980) 1202–1208
3. Mabry, C. C., Denniston, J. C., Nelson, T. L. and Choon, D. S. Maternal phenylketonuria: a cause of mental retardation in children without the metabolic defect.N. Engl. J. Med. 269 (1963) 1404–1408
4. Rouse, B., Lockhart, L., Matalon, R., Azen, C., Koch, R., Hanley, W., Levy, H., de la Cruz, F. and Friedman, E. Maternal phenylketonuria pregnancy outcome: a preliminary report of facial dysmorphology and major malformations.J. Inher. Metab. Dis. 13 (1990) 289–291
5. Smith, I., Glossop, J. and Beasley, M. Fetal damage due to maternal phenylketonuria: effects of dietary treatment and maternal phenylalanine concentrations around the time of conception. (An interim report from the UK Phenylketonuria Register)J. Inher. Metab. Dis. 13 (1990) 651–657
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