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CDC73 wt Allele

Known as: Hyperparathyroidism 2 (with Jaw Tumor) Gene, C1orf28, HPT-JT 
Human CDC73 wild-type allele is located in the vicinity of 1q25 and is approximately 132 kb in length. This allele, which encodes parafibromin… Expand
National Institutes of Health

Papers overview

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Review
2014
Review
2014
Parathyroid carcinoma has always been difficult to diagnose pathologically. In fact, most parathyroid tumors which are classified… Expand
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Review
2010
Review
2010
Primary hyperparathyroidism (HPT) results from the excessive secretion of parathyroid hormone from parathyroid tumours. While… Expand
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Highly Cited
2006
Highly Cited
2006
Parathyroid carcinoma is notoriously difficult to diagnose with confidence in borderline cases. Commonly there is a long lag time… Expand
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Highly Cited
2006
Highly Cited
2006
OBJECTIVE To investigate two patients with the hyperparathyroidism-jaw tumour (HPT-JT) syndrome and three patients with familial… Expand
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2006
2006
BACKGROUND A subset of familial isolated primary hyperparathyroidism (FIHP) is a variant of hyperparathyroidism-jaw tumour… Expand
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Highly Cited
2004
Highly Cited
2004
PURPOSE A reliable method for diagnosing parathyroid carcinoma has remained elusive over the years, resulting in its under… Expand
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Highly Cited
2004
Highly Cited
2004
Familial hyperparathyroidism is not uncommon in clinical endocrine practice. It encompasses a spectrum of disorders including… Expand
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2004
2004
The hyperparathyroidism-jaw tumor (HPT-JT) syndrome is an autosomal dominant disorder characterized by the occurrence of… Expand
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Highly Cited
2003
Highly Cited
2003
BACKGROUND We looked for mutations of the HRPT2 gene, which encodes the parafibromin protein, in sporadic parathyroid carcinoma… Expand
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Highly Cited
1995
Highly Cited
1995
The syndrome of hereditary hyperparathyroidism and jaw tumors (HPT-JT) is characterized by inheritance, in an autosomal dominant… Expand
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