Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' LICHTERKONECKI U' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 11 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. RIVERA I; LEANDRO P; LICHTERKONECKI U; DEALMEIDA IT; LECHNER MC
      POPULATION-GENETICS OF HYPERPHENYLALANINEMIA RESULTING FROM PHENYLALANINE-HYDROXYLASE DEFICIENCY IN PORTUGAL

      Journal of Medical Genetics
    2. RIVERA I; LEANDRO P; LICHTERKONECKI U; DEALMEIDA IT; LECHNER MC
      RELATIVE FREQUENCY OF IVS10NT546 MUTATION IN A PORTUGUESE PHENYLKETONURIC POPULATION

      Human mutation
    3. MCDOWELL G; ISOGAI T; TANIGAMI A; HAZELWOOD S; LEDBETTER D; POLYMEROPOULOS MH; LICHTERKONECKI U; KONECKI D; TOWN MM; VANTHOFF W; WEISSENBACH J; GAHL WA
      FINE MAPPING OF THE CYSTINOSIS GENE USING AN INTEGRATED GENETIC AND PHYSICAL MAP OF A REGION WITHIN HUMAN-CHROMOSOME BAND 17P13

      Biochemical and molecular medicine
    4. BURGARD P; RUPP A; KONECKI DS; TREFZ FK; SCHMIDT H; LICHTERKONECKI U
      PHENYLALANINE-HYDROXYLASE GENOTYPES, PREDICTED RESIDUAL ENZYME-ACTIVITY AND PHENOTYPIC PARAMETERS OF DIAGNOSIS AND TREATMENT OF PHENYLKETONURIA

      European journal of pediatrics
    5. LICHTERKONECKI U; SCHLOTTER M; KONECKI DS
      DNA-SEQUENCE POLYMORPHISMS IN EXONIC AND INTRONIC REGIONS OF THE HUMAN PHENYLALANINE-HYDROXYLASE GENE AID IN THE IDENTIFICATION OF ALLELES

      Human genetics
    6. LICHTERKONECKI U; RUPP A; KONECKI DS; TREFZ FK; SCHMIDT H; BURGARD P
      RELATION BETWEEN PHENYLALANINE-HYDROXYLASE GENOTYPES AND PHENOTYPIC PARAMETERS OF DIAGNOSIS AND TREATMENT OF HYPERPHENYLALANINAEMIC DISORDERS

      Journal of inherited metabolic disease
    7. BARIC I; MARDESIC D; SARNAVOKA V; LICHTERKONECKI U; KONECKI DS; TREFZ FK
      GEOGRAPHICAL-DISTRIBUTION OF THE P281L MUTATION AT THE PHENYLALANINE-HYDROXYLASE LOCUS - POSSIBLE ORIGIN IN SOUTHEASTERN EUROPE

      Journal of inherited metabolic disease
    8. KONECKI DS; FOETISCH K; SCHLOTTER M; LICHTERKONECKI U
      COMPLETE CDNA SEQUENCE OF HUMAN LYSOSOME-ASSOCIATED MEMBRANE PROTEIN-2

      Biochemical and biophysical research communications
    9. APOLD J; EIKEN HG; SVENSSON E; KUNERT E; KOZAK L; CECHAK P; GUTTLER F; GILTAY J; LICHTERKONECKI U; MELLE D; JARUZELSKA JM
      THE PHENYLKETONURIA G272X HAPLOTYPE-7 MUTATION IN EUROPEAN POPULATIONS

      Human genetics
    10. KONECKI DS; SCHWEITZERKRANTZ S; BYRD D; TREFZ FK; LICHTERKONECKI U
      FACILITATION OF HYPERPHENYLALANINEMIA PHENOTYPE ASSESSMENT BY GENOTYPE ANALYSIS

      European journal of pediatrics
    11. TREFZ FK; BURGARD P; KONIG T; GOEBELSCHREINER B; LICHTERKONECKI U; KONECKI D; SCHMIDT E; SCHMIDT H; BICKEL H
      GENOTYPE-PHENOTYPE CORRELATIONS IN PHENYLKETONURIA

      Clinica chimica acta


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/05/20 alle ore 09:22:57