1p32

A chromosome band present on 1p
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 testing single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) for… (More)
  • figure 1
  • table 1
  • table 2
  • table 3
  • table 4
Is this relevant?
2007
2007
Nonsyndromic defects in the urinary tract are the most common cause of end-stage renal failure in children and account for a… (More)
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Autosomal dominant hypercholesterolemia (ADH; OMIM144400), a risk factor for coronary heart disease, is characterized by an… (More)
  • figure 1
  • figure 2
Is this relevant?
Highly Cited
2002
Highly Cited
2002
Eight regions of the genome (PARK1-8) have been implicated in autosomal dominant and autosomal recessive forms of early-onset… (More)
Is this relevant?
2000
2000
Clinical familial hypercholesterolemia has been shown to result from mutations in 2 genes, the low density lipoprotein (LDL… (More)
  • table 1
  • figure 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?
Review
1999
Review
1999
Prospective studies on the detection of minimal residual disease (MRD) in acute leukemia patients have shown that large-scale MRD… (More)
  • figure 1
  • table 2
  • figure 2
  • figure 3
  • table 4
Is this relevant?
Review
1999
Review
1999
BEGINNING AT THE BEDSIDE: A CASE OF T-CELL LEUKEMIA THIS STORY BEGINS with a seminal case report describing a 16-year-old boy who… (More)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Highly Cited
1996
Highly Cited
1996
Hematopoietic development is a complex process that involves a large number of growth factors and cytokines. Many cytokines are… (More)
Is this relevant?
Highly Cited
1995
Highly Cited
1995
NEURONAL ceroid lipofuscinoses (NCL) represent a group of common progressive encephalopathies of children which have a global… (More)
Is this relevant?
1988
1988
Chromosome deletion at the short arm of one chromosome 1 (1p32)—the most common aberration in neuroblastoma cells—was found to be… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 5
Is this relevant?