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
Is this relevant?
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
Is this relevant?
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
Is this relevant?
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
Is this relevant?
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
Is this relevant?
2001
2001
We have studied cultured skin fibroblasts from three siblings and one unrelated individual, all of whom had fatal mitochondrial… Expand
Is this relevant?
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
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective… Expand
Is this relevant?
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
Is this relevant?
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
Is this relevant?