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Citation: P. Burgard et al., PHENYLALANINE-HYDROXYLASE GENOTYPES, PREDICTED RESIDUAL ENZYME-ACTIVITY AND PHENOTYPIC PARAMETERS OF DIAGNOSIS AND TREATMENT OF PHENYLKETONURIA, European journal of pediatrics, 155, 1996, pp. 11-15
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Citation: Ds. Konecki et al., AN ALTERNATIVELY SPLICED FORM OF THE HUMAN LYSOSOME-ASSOCIATED MEMBRANE PROTEIN-2 GENE IS EXPRESSED IN A TISSUE-SPECIFIC MANNER, Biochemical and biophysical research communications, 215(2), 1995, pp. 757-767
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SEDLACEK Z
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Citation: Z. Sedlacek et al., EVOLUTIONARY CONSERVATION AND GENOMIC ORGANIZATION OF XAP-4, AN XQ28 LOCATED GENE CODING FOR A HUMAN RAB GDP-DISSOCIATION INHIBITOR (GDI), Mammalian genome, 5(10), 1994, pp. 633-639
Citation: U. Lichterkonecki et al., DNA-SEQUENCE POLYMORPHISMS IN EXONIC AND INTRONIC REGIONS OF THE HUMAN PHENYLALANINE-HYDROXYLASE GENE AID IN THE IDENTIFICATION OF ALLELES, Human genetics, 94(3), 1994, pp. 307-310
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BENDER C
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Citation: C. Bender et al., METHYLMALONIC ACIDEMIA - HAPLOTYPE ANALYSIS OF THE METHYLMALONYL-COA-MUTASE GENE IN EUROPE, European journal of pediatrics, 153(6), 1994, pp. 468-468
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BENDER C
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Citation: C. Bender et al., HAPLOTYPE ANALYSIS AND A NEW MSPI-POLYMORPHISM AT THE PHENYLALANINE-HYDROXYLASE GENE IN THE ARABIAN POPULATION, European journal of pediatrics, 153(5), 1994, pp. 392-392
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BUCK D
THOMAS K
HEATHCOTT R
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Citation: D. Buck et al., SEQUENCING AND ANALYSIS OF HUMAN XQ28 GENOMIC DNA IN THE REGION OF THE RCP GCP LOCUS/, Cytogenetics and cell genetics, 67(4), 1994, pp. 332-332
Authors:
SEDLACEK Z
KONECKI DS
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KLAUCK SM
POUSTKA A
Citation: Z. Sedlacek et al., XAP-4, A NOVEL GENE CODING FOR A RAB GDP-DISSOCIATION INHIBITOR, IS CONSERVED IN EVOLUTION AND RESIDES IN A VERY GENE-RICH REGION OF XQ28, Cytogenetics and cell genetics, 67(4), 1994, pp. 356-356
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RUPP A
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Citation: U. Lichterkonecki et al., RELATION BETWEEN PHENYLALANINE-HYDROXYLASE GENOTYPES AND PHENOTYPIC PARAMETERS OF DIAGNOSIS AND TREATMENT OF HYPERPHENYLALANINAEMIC DISORDERS, Journal of inherited metabolic disease, 17(3), 1994, pp. 362-365
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BARIC I
MARDESIC D
SARNAVOKA V
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Citation: I. Baric et al., GEOGRAPHICAL-DISTRIBUTION OF THE P281L MUTATION AT THE PHENYLALANINE-HYDROXYLASE LOCUS - POSSIBLE ORIGIN IN SOUTHEASTERN EUROPE, Journal of inherited metabolic disease, 17(3), 1994, pp. 376-377
Authors:
KONECKI DS
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Citation: Ds. Konecki et al., COMPLETE CDNA SEQUENCE OF HUMAN LYSOSOME-ASSOCIATED MEMBRANE PROTEIN-2, Biochemical and biophysical research communications, 205(1), 1994, pp. 1-5
Authors:
VERKERK AJMH
DEGRAAFF E
DEBOULLE K
EICHLER EE
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MANCA A
POUSTKA A
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Citation: Ajmh. Verkerk et al., ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993), Human molecular genetics, 2(8), 1993, pp. 1348-1348
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KORN B
KONECKI DS
SIEBENHAAR R
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Citation: Z. Sedlacek et al., CONSTRUCTION OF A TRANSCRIPTION MAP OF A 300 KB REGION AROUND THE HUMAN G6PD LOCUS BY DIRECT CDNA SELECTION, Human molecular genetics, 2(11), 1993, pp. 1865-1869
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SCHWEITZERKRANTZ S
BYRD D
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Citation: Ds. Konecki et al., FACILITATION OF HYPERPHENYLALANINEMIA PHENOTYPE ASSESSMENT BY GENOTYPE ANALYSIS, European journal of pediatrics, 152(12), 1993, pp. 1048-1049