Presentation Information

[P2-06-2]Noonan Syndrome-Like Phenotype in a Patient with a BMP2 Loss-of-Function Variant

Seiji Mizuno1, Koki Nagai3,4, Toshi Tatematsu1, Natsuki Nakamura1, Shiomi Otsuji1, Tomoko Uehara1, Hiyori Ueda1, Shin Hayashi1,2, Tetsuya Niihori4, Mie Inaba1, Yoko Aoki4 (1.Department of Pediatircs and Clinical Genetics, Aichi Developmental Disability Center Hospital, Aichi, Japan, 2.Department of Medical Genetics, Institute of Developmental Research, Aichi Developmental Disability Center, Aichi, Japan, 3.Genetics Department, Kanagawa Childrenʼs Medical Center, 4.Department of Medical Genetics, Tohoku Universitiy)

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