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Records found: 2  
Your query: Author Sysno/Doc.kind = "^upol_us_auth d009251 t150m^"
  1. cytochromreduktasy
    cytochromreduktázy
    NADH, NADPH oxidoreduktasy
    cytochrom-B(5)-reduktasa
    NADPH-cytochrom c-reduktasa
    Cytochrome Reductases
    MESH
    (3) - MESH
    subject heading

    subject heading

  2. fenotyp Antley-Bixlerova syndromu
    Adrenal Hyperplasia, Congenital, Due To Cytochrome P450 Oxidoreductase Deficiency
    Antley-Bixler Syndrome
    Antley-Bixler Syndrome Type 1
    Antley-Bixler Syndrome Type 2
    Antley-Bixler Syndrome with Disordered Steroidogenesis
    Antley-Bixler Syndrome-Like Phenotype With Disordered Steroidogenesis
    Antley-Bixler Syndrome, Autosomal Dominant
    Antley-Bixler Syndrome, Autosomal Recessive
    Antley-Bixlerův syndrom
    Antley-Bixlerův syndrom typ 1
    Antley-Bixlerův syndrom typ 2
    Antleyho-Bixlerův syndrom - fenotyp
    Antleyho-Bixlerův syndrom autozomálně dominantní
    Antleyho-Bixlerův syndrom s anomáliemi genitálu a poruchou steroidogeneze
    Combined Partial Deficiency of 17-Hydroxylase and 21-Hydroxylase
    Congenital Adrenal Hyperplasia Due To Apparent Combined P450c17 and P450c21 Deficiency
    Cytochrome P450 Oxidoreductase Deficiency
    Disordered Steroidogenesis Due To Cytochrome P450 Oxidoreductase Deficiency
    fenotyp Antley Bixlerova syndromu
    Multisynostotic Osteodysgenesis
    Multisynostotic Osteodysgenesis With Long Bone Fractures
    Osteodysgenesis, Multisynostotic, With Fractures
    POR deficience
    POR Deficiency
    POR-vázaný Antleyho-Bixlerův syndrom
    Trapezoidocephaly-Synostosis Syndrome
    synostóza
    vrozené poruchy metabolismu steroidů
    NADPH-cytochrom c-reduktasa
    receptor fibroblastových růstových faktorů, typ 2
    Antley-Bixler Syndrome Phenotype
    MESH
    (4) - MESH
    subject heading

    subject heading



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