De novo variants in <scp><i>TCF7L2</i></scp> are associated with a syndromic neurodevelopmental disorderCaroline Dias, Lance H. Rodan, Elles M. J. Boon et al.|American Journal of Medical Genetics Part A|2021Cited by 25
ErratumNicole Wilson, Marcelo Ricardo Vicari, Michael Schmid et al.|Cytogenetic and Genome Research|2006Cited by 0