[P32] Chromosomal abnormality

[P-188] A genotype—phenotype correlation study for 4 patients with 3p13 deletion involving FOXP1

Keiko Yamamoto—shimojima^1,2, WATARU MATSUMURA³, TETSUYA OKAZAKI³, YOSHIHIRO MAEGAKI³, NOBUHIKO OKAMOTO⁴, TOSHIYUKI YAMAMOTO² (1.Restart Postdoctoral Fellowship, Japan Society for the Promotion of Science, Tokyo, Japan, 2.Institute of Medical Genetics, Tokyo Womens Medical University, Tokyo, Japan, 3.Department of Child Neurology, Tottori University, Yonago, Japan, 4.Department of Medical Genetics, Osaka Womens and Childrens Hospital, Osaka, Japan)