Prenatal genetic testing for a microdeletion at chromosome 14q32.2 imprinted region leading to UPD(14)pat-like phenotype†

Prenatal Genetic Testing for a Microdeletion at Chromosome 14q32.2 Imprinted Region Leading to UPD(14)pat-like Phenotype Aiko Sasaki, Masahiro Sumie, Seiji Wada, Rika Kosaki, Kenji Kurosawa, Maki Fukami, Haruhiko Sago, Tsutomu Ogata, and Masayo Kagami* Department of Maternal-Fetal and Neonatal Medicine, National Center for Child Health and Development, Tokyo, Japan Division of Medical Genetics, National Center for Child Health and Development, Tokyo, Japan Division of Medical Genetics, Kanagawa Children’s Medical Center, Yokohama, Japan Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan