Associated Papers
A novel pathogenic splice site variation in STK11 gene results in Peutz-Jeghers syndrome.
Zhao N et al.
Molecular Genetics & Genomic Medicine, 2021
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
Hearle NC et al.
Journal of Medical Genetics, 2006
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
Lim W et al.
British Journal of Cancer, 2003
Select a paper to view details