2q37

A chromosome band present on 2q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1978-2017
05101519782017

Papers overview

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2012
2012
  • Pengjie Wu, Ning Zhang, +4 authors Kan Gong
  • Journal of Human Genetics
  • 2012
Von Hippel–Lindau (VHL) disease is an autosomal dominant familial cancer syndrome caused by germline mutations in VHL tumor… (More)
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Highly Cited
2009
Highly Cited
2009
The inflammatory bowel diseases (IBD) Crohn's disease and ulcerative colitis are common causes of morbidity in children and young… (More)
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2009
2009
Familial idiopathic basal ganglia calcification (FIBGC) is an inherited neurodegenerative disorder characterized by the… (More)
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2007
2007
Overexpression of the C-type natriuretic peptide, encoded by the NPPC gene in 2q37.1, was recently reported in a patient… (More)
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2006
2006
Deletions of the 2q37 region are associated with a recognizable pattern of MCA/MR so-called the AHO-like syndrome. Brachydactyly… (More)
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Highly Cited
2000
Highly Cited
2000
To identify chromosomal regions containing susceptibility loci for systemic lupus erythematosus (SLE), we performed genome scans… (More)
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1999
Highly Cited
1999
The G protein-coupled receptor (GPCR) family share a structural motif of seven transmembrane segments with large numbers of… (More)
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1998
1998
To identify the subchromosomal region that carries the cellular-senescence-restoring program of the human cervical carcinoma cell… (More)
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1995
1995
We report five patients with a combination of brachymetaphalangia and mental retardation, similar to that observed in Albright… (More)
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1990
1990
We have demonstrated close linkage between the locus for the autosomal dominant Waardenburg syndrome type I and the placental… (More)
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