Dyshormonogenic goiter

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2011
0119842011

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Review
2011
Review
2011
BACKGROUND Mutations in the SLC26A4 gene, coding for the anion transporter pendrin, are responsible for Pendred syndrome… (More)
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Highly Cited
2008
Highly Cited
2008
CONTEXT Dual oxidase 2 (DUOX2) is the catalytic core of the H(2)O(2) generator crucial for the iodination of thyroglobulin in… (More)
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2002
2002
The disease gene for Pendred syndrome has been recently characterized and named PDS. It codes for a transmembrane protein called… (More)
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1999
1999
Pendred syndrome is the most common form of syndromic deafness, characterized by dyshormonogenic goiter associated with sensory… (More)
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1984
1984
The value of serum thyroglobulin (Tg) determination in the differential diagnosis of congenital hypothyroidism was assessed by… (More)
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