Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome.
Candy KumpsErika D'haenensJennifer KerkhofHaley McConkeyMarielle AldersBekim SadikovicOlivier M VanakkerPublished in: European journal of human genetics : EJHG (2023)