Cystic fibrosis is an autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator gene. This disorder produces a variable phenotype including lung disea
Our work aims to provide evidence that could allow clinics to consider using niPGT-A as a method in screening aneuploidies or chromosome rearrangements in blastocytes, either alone or with conventiona
BackgroundThe large number (30) of permanent human embryonic stem cell (hESC) lines and additional 29 which did not continue growing, in our laboratory at Karolinska Institutet have given us a possibi
