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7. Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio. Westwood A; Raine DN J Med Genet; 1975 Dec; 12(4):327-33. PubMed ID: 1219115 [TBL] [Abstract][Full Text] [Related]
8. [Phenylalanine level in the serum of heterozygotes for phenylketonuria under intensified protein catabolism]. Bliumina MG Genetika; 1981; 17(5):910-4. PubMed ID: 7195856 [TBL] [Abstract][Full Text] [Related]
9. Identification of heterozygotes with phenylketonuria on basis of blood tyrosine responses. ANDERSON JA; GRAVEM H; ERTEL R; FISCH R J Pediatr; 1962 Oct; 61():603-9. PubMed ID: 13861239 [No Abstract] [Full Text] [Related]
10. Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria compared with 26 normals. Thalhammer O; Pollak A; Lubec G; Königshofer H J Inherit Metab Dis; 1981; 4(2):73-4. PubMed ID: 6790854 [No Abstract] [Full Text] [Related]
11. [A new method of detection of heterozygotes in phenylpyruvic oligophrenia]. Mamelle N; Mamelle JC; Site J; Quincy C; Later R; Masson E; Moreau P; François R Rev Eur Etud Clin Biol; 1971 Apr; 16(4):342-51. PubMed ID: 5564546 [No Abstract] [Full Text] [Related]
12. Heterozygous carriers in the relatives of a case of phenylketonuria. Kääriäinen R; Karlsson R Hereditas; 1973; 75(1):109-17. PubMed ID: 4778101 [No Abstract] [Full Text] [Related]
13. [Intravenous phenylalanine loading test in normal subjects and the parents of phenylketonuretics]. Badinand A; François R; Site J; Quincy C; Mamelle N; Masson E; Later R C R Seances Soc Biol Fil; 1968; 162(8):1525-8. PubMed ID: 4238174 [No Abstract] [Full Text] [Related]
14. Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals. Thalhammer O; Pollak A; Lubec G; Königshofer H Hum Genet; 1980; 54(2):213-6. PubMed ID: 7390492 [No Abstract] [Full Text] [Related]
15. About changes of the phenylalanine-tyrosine metabolism in psoriasis vulgaris. Knapp A Acta Univ Carol Med (Praha); 1986; 32(3-4):203-6. PubMed ID: 3434474 [No Abstract] [Full Text] [Related]
16. [Intravenous loading of L-phenylalanine: detection of heterozygotes in phenylketonuria]. Lambert J; Viailhet M; Monot C; Lepoire E; Baradel J; Nabet P; Martin J; Pierson M C R Seances Soc Biol Fil; 1973; 167(3):502-8. PubMed ID: 4785089 [No Abstract] [Full Text] [Related]
17. Detection of heterozygotes for phenylketonuria by column chromatography and discriminatory analysis. Rampini S; Anders PW; Curtius HC; Marthaler T Pediatr Res; 1969 Jul; 3(4):287-97. PubMed ID: 5807058 [No Abstract] [Full Text] [Related]
18. Progress in the identification of the heterozygote in phenylketonuria. Lehmann WD J Pediatr; 1989 Jun; 114(6):915-24. PubMed ID: 2566668 [No Abstract] [Full Text] [Related]
19. Phenylketonuria: a family study. Crosby PF; Navarro A; Matos ML Bol Asoc Med P R; 1969 Apr; 61(4):133-7. PubMed ID: 5255738 [No Abstract] [Full Text] [Related]
20. A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninaemia). Woolf LI; Goodwin BL; Cranston WI; Wade DN; Woolf F; Hudson FP; McBean MS Lancet; 1968 Jan; 1(7534):114-7. PubMed ID: 4169602 [No Abstract] [Full Text] [Related] [Next] [New Search]