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Clinical Characteristics of Fragile X Syndrome Patients in Japan.
Okazaki, Tetsuya; Adachi, Kaori; Matsuura, Kaori; Oyama, Yoshitaka; Nose, Madoka; Shirahata, Emi; Abe, Toshiaki; Hasegawa, Takeshi; Maihara, Toshiro; Maegaki, Yoshihiro; Nanba, Eiji.
Afiliação
  • Okazaki T; Division of Clinical Genetics, Tottori University Hospital, Yonago 680-8504, Japan.
  • Adachi K; Research Initiative Center, Organization for Research Initiative and Promotion, Tottori University, Yonago 680-8503, Japan.
  • Matsuura K; Division of Clinical Genetics, Tottori University Hospital, Yonago 680-8504, Japan.
  • Oyama Y; Department of Pediatrics, Yokohama City University Medical Center, Yokohama 232-0024, Japan.
  • Nose M; Department of Pediatrics, Nose Pediatric Clinic, Kobe 653-0004, Japan.
  • Shirahata E; Department of Pediatrics, Yamagata Prefectural Rehabilitation Center for Children with Disabilities, Kaminoyama 990-8570, Japan.
  • Abe T; Department of Pediatrics, Ashikaganomori Hospital, Ashikaga 326-0011, Japan.
  • Hasegawa T; Department of Pediatrics, Soka Municipal Hospital, Soka 340-0043, Japan.
  • Maihara T; Department of Pediatrics, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki 660-8550, Japan.
  • Maegaki Y; Division of Clinical Genetics, Tottori University Hospital, Yonago 680-8504, Japan.
  • Nanba E; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago 680-8504, Japan.
Yonago Acta Med ; 64(1): 30-33, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33642901
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article