10p13

A chromosome band present on 10p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1983-2016
0519832016

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Highly Cited
2010
Highly Cited
2010
Although more than 20 genetic susceptibility loci have been reported for type 2 diabetes (T2D), most reported variants have small… (More)
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2008
2008
UNLABELLED Mutations of SQSTM1 are an important cause of PDB, but other genes remain to be discovered. A major susceptibility… (More)
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2004
2004
Approximately 4,000 babies with nonsyndromic cleft lip with or without cleft palate (NSCLP) are born each year in the United… (More)
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Highly Cited
2001
Highly Cited
2001
Leprosy, a chronic infectious disease caused by Mycobacterium leprae, is prevalent in India, where about half of the world's… (More)
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Highly Cited
2001
Highly Cited
2001
The BMI-1 gene is a putative oncogene belonging to the Polycomb group family that cooperates with c-myc in the generation of… (More)
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2001
2001
Paget disease of bone (PDB) is a common disorder characterized by focal abnormalities of increased and disorganized bone turnover… (More)
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Highly Cited
2000
Highly Cited
2000
Terminal deletions of chromosome 10p result in a DiGeorge-like phenotype that includes hypoparathyroidism, heart defects, immune… (More)
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1995
1995
Comparative genomic hybridization (CGH) was applied for a comprehensive screening of chromosomal aberrations in 14 transitional… (More)
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1995
1995
Rsu-1, which was isolated based on its ability to suppress transformation by v-Ras, is a highly conserved gene which shares… (More)
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1988
1988
High-resolution cytogenetics analysis of peripheral blood lymphocytes was done prospectively on 27 of 28 patients with features… (More)
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