Plasma phenylalanine and tyrosine levels revisited in heterozygotes for hyperphenylalaninaemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00711323
Reference21 articles.
1. Anderson JA, Graven H, Ertel R, Fisch R (1962) Identification of heterozygotes with phenylketonuria on basis of blood tyrosine responses.J Pediatr 61: 603?609.
2. Berry H, Sutherland B, Guest GM (1957) Phenylalanine tolerance tests on relatives of phenylketonuric children.Am J Hum Genet 9: 310?316.
3. Blau K, Summer GK, Newsome HC, Edwards CH, Mamer OA (1973) Phenylalanine loading and aromatic acid secretion in normal subjects and heterozygotes for phenylketonuria.Clin Chim Acta 45: 183?192.
4. Brown ES, Waisman HA, Swanson MA, Colwell RE, Banks ME, Gerritsen T (1973) Effects of oral contraceptives and obesity on carrier tests for phenylketonuria.Clin Chim Acta 44: 183?192.
5. Bundey S (1978) Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom.J Med Genet 15: 249?253.
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