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14q24

A chromosome band present on 14q
National Institutes of Health

Papers overview

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Review
2011
Review
2011
Primary congenital glaucoma (PCG) is an autosomal recessive disorder in children due to the abnormal development of the… 
Highly Cited
2009
Highly Cited
2009
2003
2003
Originally described by Theodore Leber in 1869, Leber congenital amaurosis (LCA, MIM 204000) is the most early and severe form of… 
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… 
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… 
Highly Cited
2000
Highly Cited
2000
Haemoglobins and myoglobins constitute related protein families that function in oxygen transport and storage in humans and other… 
Highly Cited
1998
Highly Cited
1998
Abstract Leber congenital amaurosis (LCA) is a clinically and genetically heterogeneous autosomal recessive retinal dystrophy and… 
Highly Cited
1994
Review
1993
Review
1993
Research in oncogenetics has led to the identification of two major classes of tumor‐associated genes, oncogenes and tumor… 
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…