FUKUSHIMA YOSHIMITSU

• Yokota Y, Moteki H, Nishio SY, Yamaguchi T, Wakui K, Kobayashi Y, Ohyama K, Miyazaki H, Matsuoka R, Abe S, et al. Frequency and clinical features of hearing loss caused by STRC deletions. Sci Rep. 2019. 9. 1. 4408
• Sayaka Kawashima, Akie Nakamura, Takanobu Inoue, Keiko Matsubara, Reiko Horikawa, Keiko Wakui, Kyoko Takano, Yoshimitsu Fukushima, Toshi Tatematsu, Seiji Mizuno, et al. Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients. The Journal of clinical endocrinology and metabolism. 2018. 103. 6. 2083-2088
• Morokawa H, Kamiya M, Wakui K, Kobayashi M, Kurata T, Matsuda K, Kawamura R, Kanno H, Fukushima Y, Nakazawa Y, et al. Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter. Human genome variation. 2018. 5. 6-6
• Kyoko Takano, Kazuya Goto, Mitsuo Motobayashi, Keiko Wakui, Rie Kawamura, Tomomi Yamaguchi, Yoshimitsu Fukushima, Tomoki Kosho. Early manifestations of epileptic encephalopathy, brain atrophy, and elevation of serum neuron specific enolase in a boy with beta-propeller protein-associated neurodegeneration. EUROPEAN JOURNAL OF MEDICAL GENETICS. 2017. 60. 10. 521-526
• Yoshimitsu Fukushima. Genetic counseling of HBOC and Japanese organization of HBOC. Japanese Journal of Cancer and Chemotherapy. 2017. 44. 2. 107-110

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• 2017/11 - The Japan Society of Human Genetics Award for distinguished contribution to the Japan Society of Human Genetics

日本学術会議臨床医学委員会臨床ゲノム医学分科会 ,  The National Liaison Council for Clinical Sections of Medical Genetics ,  THE JAPANESE SOCIETY OF GENETIC DIAGNOSIS AND TREATMENT ,  THE JAPANESE SOCIETY FOR GENETIC COUNSELING ,  THE JAPAN SOCIETY OF HUMAN GENETICS