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18q21.1

A chromosome band present on 18q
National Institutes of Health

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Highly Cited
2013
Highly Cited
2013
SETBP1 mutations in 658 patients with myelodysplastic syndromes, chronic myelomonocytic leukemia and secondary acute myeloid… Expand
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Highly Cited
2012
Highly Cited
2012
Personality can be thought of as a set of characteristics that influence people's thoughts, feelings and behavior across a… Expand
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Highly Cited
2009
Highly Cited
2009
While conventional LDL-C, HDL-C, and triglyceride measurements reflect aggregate properties of plasma lipoprotein fractions, NMR… Expand
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Highly Cited
2001
Highly Cited
2001
Juvenile polyposis (JP; OMIM 174900) is an autosomal dominant gastrointestinal hamartomatous polyposis syndrome in which patients… Expand
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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… Expand
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Highly Cited
1998
Highly Cited
1998
Familial juvenile polyposis (FJP) is a hamartomatouspolyposis syndrome in which affected family members develop upper and lower… Expand
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Highly Cited
1997
Highly Cited
1997
There are currently 13 diseases known to be caused by unstable triplet repeat mutations; however, there are some instances (as… Expand
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Highly Cited
1996
Highly Cited
1996
About 90 percent of human pancreatic carcinomas show allelic loss at chromosome 18q. To identify candidate tumor suppressor genes… Expand
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Highly Cited
1996
Highly Cited
1996
We recently identified a novel tumor-suppressor gene, DPC4, at chromosome 18q21.1 and found that both alleles of DPC4 were… Expand
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Highly Cited
1996
Highly Cited
1996
Absolute genetic differences between neoplastic and nonneoplastic cells can be discerned at sites of homozygous deletions. These… Expand
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