Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene
収録刊行物
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- Eur J Pediatr
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Eur J Pediatr 162 674-677, 2003
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- CRID
- 1571417125370047104
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- NII論文ID
- 10018765661
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- データソース種別
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- CiNii Articles