Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

2p13

A chromosome band present on 2p
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
We conducted a genome-wide association study of rheumatoid arthritis in 2,418 cases and 4,504 controls from North America and… Expand
  • figure 1
  • table 1
  • figure 2
Highly Cited
2003
Highly Cited
2003
Impaired axonal transport in motor neurons has been proposed as a mechanism for neuronal degeneration in motor neuron disease… Expand
  • figure 1
  • figure 2
Highly Cited
2002
Highly Cited
2002
Alström syndrome (OMIM 203800) is an autosomal recessive disease, characterized by cone–rod retinal dystrophy, cardiomyopathy and… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Highly Cited
2001
Highly Cited
2001
Mitochondrial DNA (mtDNA)–depletion syndromes (MDS; OMIM 251880) are phenotypically heterogeneous, autosomal-recessive disorders… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Highly Cited
2001
Highly Cited
2001
Carcinomas that develop in the pancreatic islets of transgenic mice expressing the SV40 T-antigens (Tag) under transcriptional… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Highly Cited
2001
Highly Cited
2001
Many malignancies of mature B cells are characterized by chromosomal translocations involving the immunoglobulin heavy chain (IGH… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Highly Cited
1999
Highly Cited
1999
Pre-eclampsia is a common and serious disease and a major cause of maternal and infant mortality. Antenatal care systems world… Expand
Highly Cited
1998
Highly Cited
1998
Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective… Expand
Highly Cited
1998
Highly Cited
1998
Miyoshi myopathy (MM) is an adult onset, recessive inherited distal muscular dystrophy that we have mapped to human chromosome… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • table 2
Highly Cited
1998
Highly Cited
1998
The limb-girdle muscular dystrophies are a genetically heterogeneous group of inherited progressive muscle disorders that affect… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 5