Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co‐activator CBFB

Tomohide Goto(Tokyo Metropolitan Children's Medical Center), Kenjiro Kosaki(Keio University), Hiroshi Yoshihashi(Tokyo Metropolitan Children's Medical Center), Yukihiro Hasegawa(Tokyo Metropolitan Children's Medical Center), Michihiko Aramaki(Asahikawa Medical College Hospital), Yoshimitsu Fukushima(Saitama Children's Medical Center), Takao Takahashi(Keio University), Takashi Ishii(Mitsubishi Group (Japan)), Gen Nishimura(Musashino University)

Congenital Anomalies

November 25, 2004

Cited by 27

|American Journal of Medical Genetics Part A|2011|717

|American Journal of Medical Genetics Part A|2019|620

|American Journal of Medical Genetics Part A|2015|570

|American Journal of Medical Genetics|1988|457

|American Journal of Medical Genetics Part A|2023|386

Large fontanelles are a shared feature of haploinsufficiency of <i>RUNX2</i> and its co‐activator <i>CBFB</i>