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2. The molecular basis of phenylalanine hydroxylase deficiency in Croatia. Zschocke J; Preusse A; Sarnavka V; Fumic K; Mardesic D; Hoffmann GF; Baric I Hum Mutat; 2003 Apr; 21(4):399. PubMed ID: 12655552 [TBL] [Abstract][Full Text] [Related]
3. An ongoing debate over phenylalanine hydroxylase deficiency in phenylketonuria. Scriver CR J Clin Invest; 1998 Jun; 101(12):2613-4. PubMed ID: 9637693 [No Abstract] [Full Text] [Related]
4. Phenylketonuria. Population genetics of a disease. Kidd KK Nature; 1987 May 28-Jun 3; 327(6120):282-3. PubMed ID: 2884567 [No Abstract] [Full Text] [Related]
5. Molecular basis of phenylketonuria in Venezuela: presence of two novel null mutations. De Lucca M; Pérez B; Desviat LR; Ugarte M Hum Mutat; 1998; 11(5):354-9. PubMed ID: 9600453 [TBL] [Abstract][Full Text] [Related]
6. [Genetical heterogeneity of phenylketonuria]. Annenkov GA Vopr Med Khim; 1982; 28(3):62-70. PubMed ID: 7048735 [TBL] [Abstract][Full Text] [Related]
7. Molecular genetic analysis of phenylketonuria and mental retardation. Woo SL Res Publ Assoc Res Nerv Ment Dis; 1991; 69():193-203. PubMed ID: 1672237 [No Abstract] [Full Text] [Related]
13. Phenylalanine and tyrosine metabolism in phenylketonuria heterozygotes: influence of different phenylalanine hydroxylase mutations. Spada M; Dianzani I; Bonetti G; Biondi A; Leone L; Giannattasio S; Ponzone A J Inherit Metab Dis; 1998 Jun; 21(3):236-9. PubMed ID: 9686365 [No Abstract] [Full Text] [Related]
14. Molecular basis of phenylketonuria and its clinical applications. DiLella AG; Woo SL Mol Biol Med; 1987 Aug; 4(4):183-92. PubMed ID: 2890077 [No Abstract] [Full Text] [Related]
15. Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients. Ozgüç M; Ozalp I; Coşkun T; Yilmaz E; Erdem H; Ayter S Turk J Pediatr; 1993; 35(1):11-4. PubMed ID: 7901929 [TBL] [Abstract][Full Text] [Related]
17. A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria. Feráková E; Ferák V; Kádasi L; Poláková H; Hejcmanová L; Pijacková A Funct Dev Morphol; 1992; 2(2):139-40. PubMed ID: 1360274 [No Abstract] [Full Text] [Related]
18. [Spectrum and methods of detection of mutations in a phenylalanine hydroxylase gene from patients with phenylketonuria from the Novosibirsk region]. Smagulova FO; Morozov IV Bioorg Khim; 2000 Nov; 26(11):838-43. PubMed ID: 11696894 [TBL] [Abstract][Full Text] [Related]
19. Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria. Jaruzelska J; Borski K; Riess O; Blin N; Słomski R Acta Biochim Pol; 1989; 36(3-4):323-32. PubMed ID: 2577230 [TBL] [Abstract][Full Text] [Related]
20. Mutations of the phenylalanine hydroxylase gene in mild hyperphenylalaninemia: a novel mutation in exon 3. Zekanowski C; Cabalska B; Borsuk P; Bal J Hum Mutat; 1997; 10(3):258-9. PubMed ID: 9298832 [No Abstract] [Full Text] [Related] [Next] [New Search]