Studies on the Molecular Diagnosis of Mowat ‒ Wilson Syndrome : The Role of Chromosomal Microarray in Approaching Syndromic Congenital Heart Defects

Yu Nakagama, MD1, 2), Ryo Inuzuka, MD, PhD1), Yu Tanaka, MD1), Kazuhiro Shiraga, MD1), Hiroko Asakai, MD1), Takahiro Shindo, MD1), Yoichiro Hirata, MD, PhD1), Junko Takita, MD, PhD1), Seishi Ogawa, MD, PhD3), and Akira Oka, MD, PhD1) 1) Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan 2) JSPS Research Fellow, Japan Society for the Promotion of Science, Tokyo, Japan 3) Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan