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Chisako Aoki

Showing results (1-10 of 5) with videos related to

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Brain & Development|October 31, 2025
Reply to: "When neutral isn't negative: missteps in survey data analysis"Tetsuya Okazaki, Chisako Aoki, Saki Shinzato, et al.
Brain & Development|May 11, 2025
Awareness and knowledge of pediatricians regarding genetic testing for Fragile X syndrome in Japan: A National Survey of Pediatricians Managing Developmental Delay/Intellectual disabilityTetsuya Okazaki, Chisako Aoki, Saki Shinzato, et al.
Brain & Development|April 26, 2025
Japanese pediatric neurologist's decision regarding genetic testing for patients with developmental delay/intellectual disability: A nationwide surveyTetsuya Okazaki, Chisako Aoki, Kaori Adachi, et al.
Yonago Acta Medica|November 29, 2023
Mastocytosis in a Case of Noonan Syndrome Caused by a De Novo Pathogenic <i>CBL</i> VariantTatsuya Kawaguchi, Tohru Okanishi, Tetsuya Okazaki, et al.
Human Genome Variation|May 17, 2022
Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletionTetsuya Okazaki, Tatsuya Kawaguchi, Yusuke Saiki, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Brain & Development|October 31, 2025
Reply to: "When neutral isn't negative: missteps in survey data analysis"Tetsuya Okazaki, Chisako Aoki, Saki Shinzato, et al.
Brain & Development|May 11, 2025
Awareness and knowledge of pediatricians regarding genetic testing for Fragile X syndrome in Japan: A National Survey of Pediatricians Managing Developmental Delay/Intellectual disabilityTetsuya Okazaki, Chisako Aoki, Saki Shinzato, et al.
Brain & Development|April 26, 2025
Japanese pediatric neurologist's decision regarding genetic testing for patients with developmental delay/intellectual disability: A nationwide surveyTetsuya Okazaki, Chisako Aoki, Kaori Adachi, et al.
Yonago Acta Medica|November 29, 2023
Mastocytosis in a Case of Noonan Syndrome Caused by a De Novo Pathogenic <i>CBL</i> VariantTatsuya Kawaguchi, Tohru Okanishi, Tetsuya Okazaki, et al.
Human Genome Variation|May 17, 2022
Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletionTetsuya Okazaki, Tatsuya Kawaguchi, Yusuke Saiki, et al.
Pageof 1