Congenital Hypothyroidism, Cerebellar Atrophy, and the Incomplete Phenotypic Expression of PHACES Syndrome
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- MUSSA Alessandro
- Pediatric Endocrinology, Department of Paediatrics, University of Torino
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- CORRIAS Andrea
- Pediatric Endocrinology, Department of Paediatrics, University of Torino
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- BALDASSARRE Giuseppina
- Clinical Genetics, Department of Paediatrics, University of Torino
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- BIAMINO Elisa
- Clinical Genetics, Department of Paediatrics, University of Torino
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- SILENGO Margherita
- Clinical Genetics, Department of Paediatrics, University of Torino
この論文をさがす
収録刊行物
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- Endocrine Journal
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Endocrine Journal 55 (1), 231-, 2008
一般社団法人 日本内分泌学会
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詳細情報 詳細情報について
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- CRID
- 1390001206298975360
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- NII論文ID
- 10021265159
- 130004443375
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- NII書誌ID
- AA10901436
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- ISSN
- 13484540
- 09188959
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles