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

14q24

A chromosome band present on 14q
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Primary congenital glaucoma (PCG) is an autosomal-recessive condition characterized by high intraocular pressure (IOP), usually… Expand
2007
2007
Bipolar disorder (BPD) is a complex genetic disorder with cycling symptoms of depression and mania. Despite the extreme… Expand
2003
2003
Originally described by Theodore Leber in 1869, Leber congenital amaurosis (LCA, MIM 204000) is the most early and severe form of… Expand
Highly Cited
2002
Highly Cited
2002
Asthma is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
Highly Cited
2001
Highly Cited
2001
Leukoencephalopathy with vanishing white matter (VWM) is an inherited brain disease that occurs mainly in children. The course is… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Highly Cited
2000
Highly Cited
2000
Haemoglobins and myoglobins constitute related protein families that function in oxygen transport and storage in humans and other… Expand
Highly Cited
1998
Highly Cited
1998
Abstract Leber congenital amaurosis (LCA) is a clinically and genetically heterogeneous autosomal recessive retinal dystrophy and… Expand
  • figure 1
  • figure 2
  • figure 3
  • table 1
Highly Cited
1994
Highly Cited
1994
Latent transforming growth factor-beta (TGF-beta)-binding protein (LTBP) is a component of the latent TGF-beta complex in human… Expand
Review
1993
Review
1993
Research in oncogenetics has led to the identification of two major classes of tumor‐associated genes, oncogenes and tumor… Expand
Highly Cited
1993
Highly Cited
1993
Cytogenetic analysis of short-term cultures from seven pulmonary hamartomas revealed an abnormal karyotype in six of them. The… Expand
  • table I
  • figure 1
  • figure 2
  • figure 3