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Mutations in the Pendred Syndrome ( PDS/SLC26A ) Gene: An Increasingly Complex Phenotypic Spectrum From Goiter to Thyroid Hypoplasia

✍ Scribed by Kopp, Peter


Book ID
126493900
Publisher
Endocrine Society
Year
2014
Tongue
English
Weight
58 KB
Volume
99
Category
Article
ISSN
0021-972X

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