3p21

A chromosome band present on 3p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1980-2017
0102019802017

Papers overview

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Highly Cited
2013
Highly Cited
2013
BACKGROUND Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Two inflammatory disorders, type 1 diabetes and celiac disease, cosegregate in populations, suggesting a common… (More)
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Highly Cited
2004
Highly Cited
2004
Nasopharyngeal carcinoma (NPC) poses one of the serious health problems in southern Chinese, with an incidence rate ranging from… (More)
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Highly Cited
2000
Highly Cited
2000
Allelic loss at the short arm of chromosome 3 is one of the most common and earliest events in the pathogenesis of lung cancer… (More)
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Highly Cited
1999
Highly Cited
1999
Two new members of a family of putative hyaluronidase genes involved in glycosaminoglycan catabolism have been identified and… (More)
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Highly Cited
1996
Highly Cited
1996
The chemokine receptor 5 (CKR5) protein serves as a secondary receptor on CD4(+) T lymphocytes for certain strains of human… (More)
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Highly Cited
1994
Highly Cited
1994
The human DNA mismatch repair gene homologue hMSH2, on chromosome 2p is involved in hereditary non-polyposis colon cancer (HNPCC… (More)
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Highly Cited
1994
Highly Cited
1994
Some cases of hereditary nonpolyposis colorectal cancer (HNPCC) are due to alterations in a mutS-related mismatch repair gene. A… (More)
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Highly Cited
1992
Highly Cited
1992
Cytogenetic abnormalities and high-frequency allele losses involving the short arm of human chromosome 3 have been identified in… (More)
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Highly Cited
1987
Highly Cited
1987
In childhood malignancies such as retinoblastoma and Wilms tumour, of which both familial and sporadic forms exist, recessive… (More)
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