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Brain & Development
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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 disability
Tetsuya 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 survey
Tetsuya 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> Variant
Tatsuya 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 deletion
Tetsuya Okazaki, Tatsuya Kawaguchi, Yusuke Saiki, et al.
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Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 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 disability
Tetsuya 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 survey
Tetsuya 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> Variant
Tatsuya 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 deletion
Tetsuya Okazaki, Tatsuya Kawaguchi, Yusuke Saiki, et al.
Page
of 1