The 60th Annual Meeting of the Japanese Society of Child Neurology

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Oral Presentation

Hereditary disorder/Chromosomal aberration

[O4] Hereditary disorder/Chromosomal aberration

Thu. May 31, 2018 2:30 PM - 3:30 PM Room 7 (3F 304)

Chair: Takeo Kubota(Faculty of Child Studies, Seitoku University), Yamamoto-Shimojima Keiko(Institute of Medical Genetics, Tokyo Women's Medical University)

[O-023] The central precocious puberty gene, Mkrn3 shows development—specific imprinting in mouse testis

Tatsuya Kishino (Division of Functional Genomics, Center for Frontier Science, Nagasaki University, Nagasaki, Japan)

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