Treffer 1 - 2 von 2 für Suche 'Gholipoorfeshkecheh, Rahim', Suchdauer: 0,45s Treffer weiter einschränken
  1. 1
    Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

    Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects von Gholipoorfeshkecheh, Rahim, Agarwala, Swati, G, Kavya, Krishnappa, Santhosh, Savitha, Mysore R, Ramachandra, Nallur B


    Volltext
    Artikel

    Zu den Favoriten
    Gespeichert in:
  2. 2
    Variants in HEY genes manifest in Ventricular Septal Defects of Congenital Heart Disease

    Variants in HEY genes manifest in Ventricular Septal Defects of Congenital Heart Disease von Gholipoorfeshkecheh, Rahim, Agarwala, Swati, Krishnappa, Santhosh, Savitha, M.R., Narayanappa, D., Ramachandra, Nallur B.

    Veröffentlicht in Gene reports

    Volltext
    Artikel

    Zu den Favoriten
    Gespeichert in:

Suchwerkzeuge: