A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia MRI and clinical characteristics of suspected cerebrovascular accident in nine cats Distinct cerebellar foliation anomalies in a Chd7 haploinsufficient mouse model of CHARGE syndrome The chromatin remodeling factor CHD7 controls cerebellar development by regulating reelin expression View all publications