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3. Mutation screening of phenylketonuria in the Far East of Russia. Sueoka H; Moshinetsky A; Nagao M; Chiba S J Hum Genet; 1999; 44(6):368-71. PubMed ID: 10570906 [TBL] [Abstract][Full Text] [Related]
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6. 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]
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9. Frequencies of the most common mutations responsible for phenylketonuria in Poland. Zekanowski C; Nowacka M; Zgulska M; Horst J; Cabalska B; Mazurczak T Mol Cell Probes; 1994 Aug; 8(4):323-4. PubMed ID: 7870074 [TBL] [Abstract][Full Text] [Related]
11. Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal. Rivera I; Leandro P; Lichter-Konecki U; Tavares de Almeida I; Lechner MC J Med Genet; 1998 Apr; 35(4):301-4. PubMed ID: 9598724 [TBL] [Abstract][Full Text] [Related]
12. 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]
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20. [Analysis of mutations in the phenylalanine hydroxylase gene in Ukrainian families at high risk for phenylketonuria]. Nechiporenko MV; Lalivshits LA Tsitol Genet; 2000; 34(6):59-63. PubMed ID: 11391893 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]