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Chromosomes, Human, Pair 3

Known as: 3 chromosome, 3 chromosomes, Chromosome 3 
The designation for each member of the third largest human autosomal chromosome pair. Chromosome 3 spans almost 200 million base pairs and represents… Expand
National Institutes of Health

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Highly Cited
2009
Highly Cited
2009
Drug-induced liver injury (DILI) is an important cause of serious liver disease. The antimicrobial agent flucloxacillin is a… Expand
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Highly Cited
2006
Highly Cited
2006
The GS3 locus located in the pericentromeric region of rice chromosome 3 has been frequently identified as a major QTL for both… Expand
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Highly Cited
2005
Highly Cited
2005
We have previously reported a large Danish pedigree with autosomal dominant frontotemporal dementia (FTD) linked to chromosome 3… Expand
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Highly Cited
2004
Highly Cited
2004
Melanomas are notoriously difficult to classify because of a lack of discrete clinical and pathological stages. Here, we show… Expand
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Highly Cited
1996
Highly Cited
1996
BACKGROUND A high proportion of patients with uveal melanoma die of metastatic disease. In a subgroup of uveal melanomas there is… Expand
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Highly Cited
1995
Highly Cited
1995
Homozygous loss of the warts (wts) gene of Drosophila, caused by mitotic recombination in somatic cells, leads to the formation… Expand
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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… Expand
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Highly Cited
1990
Highly Cited
1990
MICE homozygous for the recessive mutation osteopetrosis (op) on chromosome 3 have a restricted capacity for bone remodelling… Expand
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Highly Cited
1990
Highly Cited
1990
Osteopetrotic (op/op) mutant mice suffer from congenital osteopetrosis due to a severe deficiency of osteoclasts. Furthermore… Expand
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Highly Cited
1990
Highly Cited
1990
THE gene for autosomal dominant retinitis pigmentosa in a large pedigree of Irish origin has recently been found to be linked to… Expand
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