Global ETD Search

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Showing 1 to 3 of 3 for “"Atrioventricular septal defects"”.

  1. A Search For Genetic Modifiers Responsible For Congenital Heart Disease Variability In The Presence Of Nkx2-5 Haploinsufficiency

    … C57Bl/6 frequently have atrial and ventricular septal defects. The incidences are substantially reduced in the Nkx2-5+/- progeny of first-generation: F1) outcrosses to the strains FVB/N or A/J. Defects recur in the second generation: F2) of the F1xF1 intercross or backcrosses to the parental …

    wustl Repository record for A Search For Genetic Modifiers Responsible For Congenital Heart Disease Variability In The Presence Of Nkx2-5 Haploinsufficiency (opens in a new tab)

  2. Integrated approaches to elucidate the genetic architecture of congenital heart defects

    Congenital heart defects (CHD) are structural anomalies affecting the heart, are found in 1% of the population and arise during early stages of embryo development. Without surgical and medical interventions, most of the severe CHD cases would not survive after the first year of life. The improved …

    cambridge Repository record for Integrated approaches to elucidate the genetic architecture of congenital heart defects (opens in a new tab)