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Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect.
Jo, Wakako; Ishizu, Katsura; Fujieda, Kenji; Tajima, Toshihiro.
Affiliation
  • Jo W; Department of Pediatrics, Hokkaido University School of Medicine, N15, W7, Sapporo, Hokkaido 060-8638, Japan.
J Thyroid Res ; 2010: 619013, 2010.
Article in En | MEDLINE | ID: mdl-21048839
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: J Thyroid Res Year: 2010 Document type: Article Affiliation country: Japan Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: J Thyroid Res Year: 2010 Document type: Article Affiliation country: Japan Country of publication: United States