Diverse transcriptional initiation revealed by fine, large‐scale mapping of mRNA start sitesYutaka Suzuki, Sumio Sugano, Hirotoshi Taira et al.|EMBO Reports|2001Cited by 161
A recurrent de novo <i>FAM111A</i> mutation causes kenny–caffey syndrome type 2Tsuyoshi Isojima, Sachiko Kitanaka, Etsuro Tokuhiro et al.|Journal of Bone and Mineral Research|2013Cited by 89