Yukiko Kuroda

Microdeletion of 19p13.3 in a girl with Peutz–Jeghers syndrome, intellectual disability, hypotonia, and distinctive features

Yukiko Kuroda, Toshiyuki Saito, Jun‐ichi Nagai et al. · American Journal of Medical Genetics Part A · 2014 · 47 citations

De novo duplication of 17p13.1–p13.2 in a patient with intellectual disability and obesity

Yukiko Kuroda, Ikuko Ohashi, Makiko Tominaga et al. · American Journal of Medical Genetics Part A · 2014 · 46 citations

Deletion of <i>UBE3A</i> in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2

Yukiko Kuroda, Ikuko Ohashi, Toshiyuki Saito et al. · American Journal of Medical Genetics Part A · 2014 · 43 citations

A postzygotic <i>NRAS</i> mutation in a patient with Schimmelpenning syndrome

Yukiko Kuroda, Ikuko Ohashi, Yumi Enomoto et al. · American Journal of Medical Genetics Part A · 2015 · 34 citations

Neuropsychology, Corticobasal Degeneration, Genetics +21

Update of the genotype and phenotype of<scp><i>KMT2D</i></scp>and<scp><i>KDM6A</i></scp>by genetic screening of 100 patients with clinically suspected Kabuki syndrome

Hiroaki Murakami, Yoshinori Tsurusaki, Keisuke Enomoto et al. · American Journal of Medical Genetics Part A · 2020 · 34 citations