Your request: (keywords:(("Genetisch bedingte Krankheit" "Chromosomenaberration" "Down-Syndrom" "Down syndrome" "Down syndrome" "Down Syndrome (D004314)" "syndrome de Down" "Fragiles-X-Syndrom" "fragile X syndrome" "Fragile X Syndrome (D005600)" "syndrome de l'X fragile" "Fragile X syndrome" "Klinefelter-Syndrom" "XYY Karyotype" "XYY karyotype" "XYY Karyotype (D014997)" "Ullrich-Turner-Syndrom" "Chromosome abnormalities" "chromosome abnormalities" "Chromosome Aberrations (D002869)" "anomalie chromosomique" "Geschlechtsgebundene Krankheit" "Fragiles-X-Syndrom" "fragile X syndrome" "Fragile X Syndrome (D005600)" "syndrome de l'X fragile" "Fragile X syndrome" "Hämophilie" "Hemophilia" "hemophilia" "Hemophilia A (D006467)" "hémophilie" "Muskeldystrophie Duchenne" "Duchenne muscular dystrophy" "Duchenne muscular dystrophy" "Muscular Dystrophy, Duchenne (D020388)" "dystrophie musculaire" "sex linked defects" "maladie liée au sexe" "Monogene Krankheit" "Chorea Huntington" "Huntington's disease" "Huntington Disease (D006816)" "maladie de Huntington" "Huntington disease" "Hämophilie" "Hemophilia" "hemophilia" "Hemophilia A (D006467)" "hémophilie" "Muskeldystrophie Duchenne" "Duchenne muscular dystrophy" "Duchenne muscular dystrophy" "Muscular Dystrophy, Duchenne (D020388)" "dystrophie musculaire" "Phenylketonurie" "Phenylketonuria" "phenylketonuria" "Phenylketonurias (D010661)" "phénylcétonurie" "Sichelzellenanämie" "Sickle cell anemia" "sickle cell anemia" "anémie à cellules falciformes" "Anemia, Sickle Cell (D000755)" "Tay-Sachs-Krankheit" "Tay Sachs disease" "Tay Sachs disease" "Tay-Sachs Disease (D013661)" "Thalassämie" "Thalassemia" "thalassemia" "Thalassemia (D013789)" "thalassémie" "Zystische Fibrose" "Cystic fibrosis" "cystic fibrosis" "Cystic Fibrosis (D003550)" "mucoviscidose" "single gene defects" "maladie monogénique" "Spätmanifeste Krankheit" "Chorea Huntington" "Huntington's disease" "Huntington Disease (D006816)" "maladie de Huntington" "Huntington disease" "Late-onset disorders" "late-onset disorders" "Age of Onset (D017668)" "maladie à révélation tardive" "Genetic disorders" "genetic disorders" "hereditary diseases" "Genetic Diseases, Inborn (D030342)" "maladie héréditaire")) OR keywords:(("genetic disorders" "chromosome aberrations" "Down syndrome" "Down syndrome" "Down syndrome" "Down Syndrome (D004314)" "syndrome de Down" "fragile X syndrome" "fragile X syndrome" "Fragile X Syndrome (D005600)" "syndrome de l'X fragile" "Fragile X syndrome" "Ullrich Turner syndrome" "XYY karyotype" "XYY Karyotype" "XYY karyotype" "XYY Karyotype (D014997)" "Chromosome abnormalities" "chromosome abnormalities" "Chromosome Aberrations (D002869)" "anomalie chromosomique" "late-onset disorders" "Huntington disease" "Huntington's disease" "Huntington Disease (D006816)" "maladie de Huntington" "Huntington disease" "Late-onset disorders" "late-onset disorders" "Age of Onset (D017668)" "maladie à révélation tardive" "sex-linked diseases" "Duchenne muscular dystrophy" "Duchenne muscular dystrophy" "Duchenne muscular dystrophy" "Muscular Dystrophy, Duchenne (D020388)" "dystrophie musculaire" "fragile X syndrome" "fragile X syndrome" "Fragile X Syndrome (D005600)" "syndrome de l'X fragile" "Fragile X syndrome" "haemophilia" "Hemophilia" "hemophilia" "Hemophilia A (D006467)" "hémophilie" "sex linked defects" "maladie liée au sexe" "single gene disorders" "cystic fibrosis" "Cystic fibrosis" "cystic fibrosis" "Cystic Fibrosis (D003550)" "mucoviscidose" "Duchenne muscular dystrophy" "Duchenne muscular dystrophy" "Duchenne muscular dystrophy" "Muscular Dystrophy, Duchenne (D020388)" "dystrophie musculaire" "haemophilia" "Hemophilia" "hemophilia" "Hemophilia A (D006467)" "hémophilie" "Huntington disease" "Huntington's disease" "Huntington Disease (D006816)" "maladie de Huntington" "Huntington disease" "phenylketonuria" "Phenylketonuria" "phenylketonuria" "Phenylketonurias (D010661)" "phénylcétonurie" "sickle cell anaemia" "Sickle cell anemia" "sickle cell anemia" "anémie à cellules falciformes" "Anemia, Sickle Cell (D000755)" "Tay Sachs disease" "Tay Sachs disease" "Tay Sachs disease" "Tay-Sachs Disease (D013661)" "thalassaemia" "Thalassemia" "thalassemia" "Thalassemia (D013789)" "thalassémie" "single gene defects" "maladie monogénique" "Genetic disorders" "genetic disorders" "hereditary diseases" "Genetic Diseases, Inborn (D030342)" "maladie héréditaire")) OR keywords:("maladie h�r�ditaire") )
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