Commentary on 'Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome'

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概要

• 論文の詳細を見る
• 2011-01-01

著者

• OKAMOTO Nobuhiko

  Osaka Medical Center and Research Institute for Maternal and Child Health

• Okamoto Nobuhiko

  Osaka Medical Center And Research Institute For Maternal And Child Health Medicat Genetics

関連論文

• Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome
• Malignant retroperitoneal tumor arising in a multicystic dysplastic kidney of a girl with Schinzel-Giedion syndrome
• Commentary on 'Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome'

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