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5. [Heterozygote identification in phenylketonuria]. Rampini S; Anders PW; Curtius HC; Marthaler T Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1968; 43(3-4):suppl 102-3. PubMed ID: 5761621 [No Abstract] [Full Text] [Related]
6. 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]
7. [Some indices of phenylalanine and tyrosine metabolism in children with phenylketonuria]. D'iachkova AIa; Lebedev BV Vopr Okhr Materin Det; 1969; 14(7):29-32. PubMed ID: 5367726 [No Abstract] [Full Text] [Related]
8. A new variant form of phenylketonuria. Watts RW; Purkiss P; Chalmers RA Q J Med; 1979 Jul; 48(191):403-17. PubMed ID: 317358 [TBL] [Abstract][Full Text] [Related]
9. [Fetal brain damage in maternal heterozygous phenylketonuria]. Kutter D; Humbel R; Metz H Med Klin; 1970 Apr; 65(14):653-6. PubMed ID: 5507797 [No Abstract] [Full Text] [Related]
10. Detection of heterozygotes for phenylketonuria. Total body phenylalanine clearance and concentrations of phenylalanine and tyrosine in the plasms of fasting subjects compared. Jagenburg R; Regårdh CG; Rödjer S Clin Chem; 1977 Sep; 23(9):1654-60. PubMed ID: 890909 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Effects of oral contraceptives and obesity on carrier tests for phenylketonuria. Brown ES; Waisman HA; Swanson MA; Colwell RE; Banks ME; Gerritsen T Clin Chim Acta; 1973 Mar; 44(2):183-92. PubMed ID: 4699626 [No Abstract] [Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. Phenylalanine metabolism and intellectual functioning among carriers of phenylketonuria and hyperphenylalaninaemia. Ford RC; Berman JL Lancet; 1977 Apr; 1(8015):767-71. PubMed ID: 66568 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. 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] [Next] [New Search]