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14q24

A chromosome band present on 14q
National Institutes of Health

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Highly Cited
2009
Highly Cited
2009
Primary congenital glaucoma (PCG) is an autosomal-recessive condition characterized by high intraocular pressure (IOP), usually… Expand
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Highly Cited
2008
Highly Cited
2008
Gene amplifications and deletions are frequent in head and neck squamous cell carcinomas (SCC) but the association of these… Expand
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2003
2003
Originally described by Theodore Leber in 1869, Leber congenital amaurosis (LCA, MIM 204000) is the most early and severe form of… Expand
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2003
2003
Mutations in hepatocyte nuclear factor (HNF)-1alpha (MODY3) account for the largest proportion of maturity-onset diabetes of the… Expand
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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
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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
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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
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Highly Cited
1998
Highly Cited
1998
Abstract Leber congenital amaurosis (LCA) is a clinically and genetically heterogeneous autosomal recessive retinal dystrophy and… Expand
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Review
1993
Review
1993
Research in oncogenetics has led to the identification of two major classes of tumor-associated genes, oncogenes and tumor… Expand
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1993
1993
Cytogenetic analysis of short-term cultures from seven pulmonary hamartomas revealed an abnormal karyotype in six of them. The… Expand
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