anchor instance (Q102986)

From ScienceSource
Jump to: navigation, search
No description defined
edit
Language Label Description Also known as
English
anchor instance
No description defined

    Statements

    PSIS phenotype through digenic inheritance, as previously demonstrated in idiopathic hypogonadotropic
    0 references
    and Kallmann syndrome ([12], [25]). Further studies are needed to elucidate in more detail the role
    0 references
    316
    0 references
    17
    0 references
    24,838
    0 references
    17 April 2019
    0 references
    0 references
    Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome. (5505202)
    0 references
     
    edit
      edit
        edit
          edit
            edit
              edit