Congenital goiter

Known as: GOITER CONGENITAL, familial goiter, GOITRE CONGENITAL 
An enlargement of the thyroid gland with congenital onset. [HPO:probinson]
National Institutes of Health

Papers overview

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Review
2010
Review
2010
Thyroglobulin (TG) defects due to TG gene mutations have an estimated incidence of approximately 1 in 100,000 newborns. This… (More)
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1999
1999
We analyzed the thyroglobulin (Tg) gene of 2 unrelated patients with congenital goiter and the Tg gene of 2 siblings with the… (More)
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1998
1998
A very large cervical tumor that extended to the upper mediastinum was seen in a newborn after an uneventful pregnancy. The… (More)
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1996
1996
In humans, deficient thyroglobulin (Tg, the thyroid prohormone) is an important cause of congenital hypothyroid goiter; further… (More)
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1992
1992
Thyroid peroxidase (TPO) is the key enzyme in the synthesis of thyroid hormones, and the TPO defects are believed to be the most… (More)
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1991
1991
A case of congenital goiter with defective thyroglobulin synthesis has been studied in molecular terms. The patient is the fifth… (More)
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Review
1991
Review
1991
 
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1987
1987
Congenital goiter (cog), a new autosomal recessive mutation in mice, has been mapped to the central region of chromosome 15… (More)
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1987
1987
Rat thyroglobulin (TG) cDNA clones were used to identify DNA restriction fragment variants among inbred mouse strains. One of… (More)
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