Hamartomatous polyposis

Known as: Hamartomatous Polyp, Hamartomatous polyps 
A polyp characterized by an overgrowth of mature cells and tissues that normally occur in the affected area.
National Institutes of Health

Papers overview

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2013
2013
Hamartomas are tumour-like malformations, consisting of disorganized normal tissues, typical of the site of tumour manifestation… (More)
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Review
2007
Review
2007
The hamartomatous polyposis syndromes are a heterogeneous group of disorders that share an autosomal-dominant pattern of… (More)
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2002
2002
Peutz-Jeghers syndrome (PJS) is a hereditary disorder characterized by gastrointestinal hamartomatous polyposis associated with… (More)
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Highly Cited
2000
Highly Cited
2000
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by melanocytic macules, hamartomatous polyps and an… (More)
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Highly Cited
1998
Highly Cited
1998
Familial juvenile polyposis is an autosomal dominant disease characterized by a predisposition to hamartomatous polyps and… (More)
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Highly Cited
1998
Highly Cited
1998
Peutz-Jeghers (PJ) syndrome is an autosomal-dominant disorder characterized by melanocytic macules of the lips, multiple… (More)
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Highly Cited
1998
Highly Cited
1998
Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease characterized by mucocutaneous pigmentation and hamartomatous… (More)
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Highly Cited
1997
Highly Cited
1997
Many human cancer susceptibility genes have been successfully mapped by genetic linkage studies1. One that has so far eluded… (More)
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Review
1995
Review
1995
Most radiologists are familiar with the clinical and radiologic features of the familial adenomatous polyposis syndromes [1]. The… (More)
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1993
1993
PURPOSE AND METHODS To clarify the potential for malignancy of Peutz-Jeghers polyposis, we investigated 75 gastrointestinal… (More)
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