These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
196 related articles for article (PubMed ID: 2564729)
1. Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency. Lyonnet S; Caillaud C; Rey F; Berthelon M; Frézal J; Rey J; Munnich A Am J Hum Genet; 1989 Apr; 44(4):511-7. PubMed ID: 2564729 [TBL] [Abstract][Full Text] [Related]
2. Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus. Berthelon M; Caillaud C; Rey F; Labrune P; Melle D; Feingold J; Frézal J; Briard ML; Farriaux JP; Guibaud P Hum Genet; 1991 Feb; 86(4):355-8. PubMed ID: 1671847 [TBL] [Abstract][Full Text] [Related]
3. CpG dinucleotides are mutation hot spots in phenylketonuria. Abadie V; Lyonnet S; Maurin N; Berthelon M; Caillaud C; Giraud F; Mattei JF; Rey J; Rey F; Munnich A Genomics; 1989 Nov; 5(4):936-9. PubMed ID: 2574153 [TBL] [Abstract][Full Text] [Related]
4. Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy. Dianzani I; Devoto M; Camaschella C; Saglio G; Ferrero GB; Cerone R; Romano C; Romeo G; Giovannini M; Riva E Hum Genet; 1990 Nov; 86(1):69-72. PubMed ID: 1979309 [TBL] [Abstract][Full Text] [Related]
5. An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2. DiLella AG; Marvit J; Brayton K; Woo SL Nature; 1987 May 28-Jun 3; 327(6120):333-6. PubMed ID: 2884570 [TBL] [Abstract][Full Text] [Related]
6. Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France. Rey F; Berthelon M; Caillaud C; Lyonnet S; Abadie V; Blandin-Savoja F; Feingold J; Saudubray JM; Frézal J; Munnich A Am J Hum Genet; 1988 Dec; 43(6):914-21. PubMed ID: 2904221 [TBL] [Abstract][Full Text] [Related]
7. The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations. Konecki DS; Lichter-Konecki U Hum Genet; 1991 Aug; 87(4):377-88. PubMed ID: 1679029 [TBL] [Abstract][Full Text] [Related]
8. [Analysis of RFLP haplotypes and point mutations at the phenylalanine hydroxylase (PAH) locus in PKU families from north China]. Fang B Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):46-50. PubMed ID: 1350519 [TBL] [Abstract][Full Text] [Related]
9. Genetic background of clinical homogeneity of phenylketonuria in Poland. Jaruzelska J; Matuszak R; Lyonnet S; Rey F; Rey J; Filipowicz J; Borski K; Munnich A J Med Genet; 1993 Mar; 30(3):232-4. PubMed ID: 8097262 [TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of PKU in eastern Europe: a nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene. Wang T; Okano Y; Eisensmith RC; Fekete G; Schuler D; Berencsi G; Nasz I; Woo SL Somat Cell Mol Genet; 1990 Jan; 16(1):85-90. PubMed ID: 2309142 [TBL] [Abstract][Full Text] [Related]
11. Phenylketonuria in the Greek population. Haplotype analysis of the phenylalanine hydroxylase gene and identification of a PKU mutation. Hofman KJ; Antonarakis SE; Missiou-Tsangaraki S; Boehm CD; Valle D Mol Biol Med; 1989 Jun; 6(3):245-50. PubMed ID: 2615649 [TBL] [Abstract][Full Text] [Related]
12. Recurrent mutation in the human phenylalanine hydroxylase gene. Okano Y; Wang T; Eisensmith RC; Güttler F; Woo SL Am J Hum Genet; 1990 May; 46(5):919-24. PubMed ID: 1971144 [TBL] [Abstract][Full Text] [Related]
13. RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families. Meijer H; Jongbloed RJ; Hekking M; Spaapen LJ; Geraedts JP Hum Genet; 1993 Dec; 92(6):588-92. PubMed ID: 7903270 [TBL] [Abstract][Full Text] [Related]
14. DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population. Lichter-Konecki U; Schlotter M; Yaylak C; Ozgüç M; Coskun T; Ozalp I; Wendel U; Batzler U; Trefz FK; Konecki D Hum Genet; 1989 Mar; 81(4):373-6. PubMed ID: 2564839 [TBL] [Abstract][Full Text] [Related]
15. [Molecular genetic aspects of phenylketonuria (PKU)]. Giltay JC; van Hoef AM; de Weger R; Duran M; Berger R; Beemer FA Tijdschr Kindergeneeskd; 1991 Jun; 59(3):77-80. PubMed ID: 1677790 [TBL] [Abstract][Full Text] [Related]
16. Linkage disequilibrium between mutation and RFLP haplotype at the phenylalanine hydroxylase locus in the German population. Lichter-Konecki U; Schlotter M; Konecki DS; Labeit S; Woo SL; Trefz FK Hum Genet; 1988 Apr; 78(4):347-52. PubMed ID: 2896156 [TBL] [Abstract][Full Text] [Related]
17. Novel PKU mutation on haplotype 2 in French-Canadians. John SW; Rozen R; Laframboise R; Laberge C; Scriver CR Am J Hum Genet; 1989 Dec; 45(6):905-9. PubMed ID: 2574002 [TBL] [Abstract][Full Text] [Related]
18. Phenylalanine hydroxylase deficiency: molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients. Rivera I; Mendes D; Afonso Â; Barroso M; Ramos R; Janeiro P; Oliveira A; Gaspar A; Tavares de Almeida I Mol Genet Metab; 2011; 104 Suppl():S86-92. PubMed ID: 21871829 [TBL] [Abstract][Full Text] [Related]
19. Mutation Analysis in Classical Phenylketonuria Patients Followed by Detecting Haplotypes Linked to Some PAH Mutations. Dehghanian F; Silawi M; Tabei SM Clin Lab; 2017 Feb; 63(2):295-300. PubMed ID: 28182360 [TBL] [Abstract][Full Text] [Related]
20. Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria. Güttler F; Ledley FD; Lidsky AS; DiLella AG; Sullivan SE; Woo SL J Pediatr; 1987 Jan; 110(1):68-71. PubMed ID: 2878985 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]