Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletion.

Okazaki, Tetsuya; Kawaguchi, Tatsuya; Saiki, Yusuke; Aoki, Chisako; Kasagi, Noriko; Adachi, Kaori; Saida, Ken; Matsumoto, Naomichi; Nanba, Eiji; Maegaki, Yoshihiro

Okazaki, Tetsuya; Kawaguchi, Tatsuya; Saiki, Yusuke; Aoki, Chisako; Kasagi, Noriko; Adachi, Kaori; Saida, Ken; Matsumoto, Naomichi; Nanba, Eiji; Maegaki, Yoshihiro.

Afiliación

Okazaki T; Division of Clinical Genetics, Tottori University Hospital, Yonago, Japan. t-okazaki@tottori-u.ac.jp.
Kawaguchi T; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan.
Saiki Y; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan.
Aoki C; Division of Clinical Genetics, Tottori University Hospital, Yonago, Japan.
Kasagi N; Division of Clinical Genetics, Tottori University Hospital, Yonago, Japan.
Adachi K; Department of Fundamental Nursing, School of Health Science, Tottori University Faculty of Medicine, Yonago, Japan.
Saida K; Division of Clinical Genetics, Tottori University Hospital, Yonago, Japan.
Matsumoto N; Research Initiative Center, Organization for Research Initiative and Promotion, Tottori University, Yonago, Japan.
Nanba E; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Maegaki Y; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Hum Genome Var ; 9(1): 14, 2022 May 17.

Article en En | MEDLINE | ID: mdl-35581197

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2022 Tipo del documento: Article País de afiliación: Japón

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