Presentation Information
[P2-01-23]18p11 and 21q11-q21 deletion due to a paternal reciprocal translocation leading to holoprosencephaly
○Hiroko Wakabayashi1, Ayumi Matsumoto2,3, Sakiko Komori3, Toshihiro Tajima3, Takayoshi Matsumura2, Takanori Yamagata3 (1.Division of Clinical Trial, Clinical Investigation Center, Jichi Medical University Hospital, Tochigi, Japan, 2.Division of Human Genetics, Center for Molecular Medicine, Jichi Medical University, Tochigi, Japan, 3.Department of Pediatrics, Jichi Medical University, Tochigi, Japan)