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20p12

A chromosome band present on 20p
National Institutes of Health

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Highly Cited
2011
Highly Cited
2011
Colorectal cancer is the second leading cause of cancer death in developed countries. Genome-wide association studies (GWAS) have… Expand
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Highly Cited
2008
Highly Cited
2008
PURPOSE Early/initiating oncogenic mutations have been identified for many cancers, but such mutations remain unidentified in… Expand
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2004
2004
Glaucoma is a leading cause of blindness worldwide. The disease is characterized by a degeneration of the optic nerve, which is… Expand
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Highly Cited
2003
Highly Cited
2003
Osteoporotic fractures are a major cause of morbidity and mortality in ageing populations. Osteoporosis, defined as low bone… Expand
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Highly Cited
2002
Highly Cited
2002
Bardet-Biedl syndrome (BBS, OMIM 209900) is a genetic disorder with the primary features of obesity, pigmentary retinopathy… Expand
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Highly Cited
2000
Highly Cited
2000
A.M.Slavotinek et al.Nature Genet. 26, 15–16 (2001). Two recent reports1,2 describing mutations in the gene for McKusick-Kaufman… Expand
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Highly Cited
1998
Highly Cited
1998
Systemic lupus erythematosus (SLE) is an autoimmune multisystem inflammatory disease characterized by the production of… Expand
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Highly Cited
1997
Highly Cited
1997
Alagille syndrome is an autosomal dominant disorder characterized by abnormal development of liver, heart, skeleton, eye, face… Expand
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Highly Cited
1997
Highly Cited
1997
Alagille syndrome (AGS) is an autosomal-dominant disorder characterized by intrahepatic cholestasis and abnormalities of heart… Expand
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Highly Cited
1997
Highly Cited
1997
Chromosomal synteny between the mouse model and humans was used to map a gene for the complex trait of obesity. Analysis of NZB… Expand
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