Endocrinopathies in a boy with cryptic copy-number variations on 4q, 7q and Xp.

Okuno, Misako; Ogata, Tsutomu; Nakabayashi, Kazuhiko; Urakami, Tatsuhiko; Fukami, Maki; Nagasaki, Keisuke

Okuno, Misako; Ogata, Tsutomu; Nakabayashi, Kazuhiko; Urakami, Tatsuhiko; Fukami, Maki; Nagasaki, Keisuke.

Afiliação

Okuno M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan; Department of Pediatrics, Nihon University School of Medicine, Tokyo, Japan.
Ogata T; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Nakabayashi K; Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development , Tokyo, Japan.
Urakami T; Department of Pediatrics, Nihon University School of Medicine , Tokyo, Japan.
Fukami M; Department of Molecular Endocrinology, National Research Institute for Child Health and Development , Tokyo, Japan.
Nagasaki K; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan; Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Hum Genome Var ; 2: 15020, 2015.

Article em En | MEDLINE | ID: mdl-27081533

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article