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10p13

A chromosome band present on 10p
National Institutes of Health

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4 relations
CELF2 wt AlleleChromosome 10 Short ArmChromosomesDCLRE1C wt Allele

Papers overview

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Highly Cited
2012
Highly Cited
2012
A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.
Review
2012
Review
2012
Pathogenesis of Paget Disease of Bone
Paget disease of bone (PDB) is a common disease characterized by focal areas of increased and disorganized bone turnover. Some… 
Review
2010
Review
2010
Leprosy and the Human Genome
SUMMARY Despite the availability of effective treatment for several decades, leprosy remains an important medical problem in many… 
Highly Cited
2008
Highly Cited
2008
CAMK1D amplification implicated in epithelial–mesenchymal transition in basal‐like breast cancer
Highly Cited
2004
Highly Cited
2004
Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.
Research to identify predisposing genes for complex diseases relying solely on clinical diagnosis is probably not ideal. Here, we… 
Review
2002
Review
2002
Refsum's disease: a peroxisomal disorder affecting phytanic acid α‐oxidation
Refsum's disease (hereditary motor sensory neuropathy type IV, heredopathia atactica polyneuritiformis) is an autosomal recessive… 
Highly Cited
2001
Highly Cited
2001
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.
Paget disease of bone (PDB) is a common disorder characterized by focal abnormalities of increased and disorganized bone turnover… 
1994
1994
Chromosome aberrations in four ependymomas.
Highly Cited
1990
Highly Cited
1990
The CEPH consortium primary linkage map of human chromosome 10.
Highly Cited
1988
Highly Cited
1988
Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
High-resolution cytogenetics analysis of peripheral blood lymphocytes was done prospectively on 27 of 28 patients with features… 
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