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19q13.3

A chromosome band present on 19q
National Institutes of Health

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Highly Cited
2005
Highly Cited
2005
The presence of common genomic deletions in the 19q13 chromosomal region in neuroblastomas and gliomas strongly suggests the… Expand
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Highly Cited
2003
Highly Cited
2003
Prostate cancer (CaP) is a common disorder with multiple genetic and environmental factors contributing to the disease. CaP… Expand
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Highly Cited
2001
Highly Cited
2001
The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal recessive disorders presenting in infancy with… Expand
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Highly Cited
2001
Highly Cited
2001
The limb girdle and congenital muscular dystrophies (LGMD and CMD) are characterized by skeletal muscle weakness and dystrophic… Expand
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Highly Cited
2001
Highly Cited
2001
We describe here a previously unknown, dominantly inherited, late-onset basal ganglia disease, variably presenting with… Expand
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Highly Cited
1999
Highly Cited
1999
Allelic alterations of chromosomes 1 and 19 are frequent events in human diffuse gliomas and have recently proven to be strong… Expand
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Highly Cited
1999
Highly Cited
1999
Mammalian polynucleotide kinases catalyze the 5′-phosphorylation of nucleic acids and can have associated 3′-phosphatase activity… Expand
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Highly Cited
1997
Highly Cited
1997
The otd/Otx gene family encodes paired-like homeodomain proteins that are involved in the regulation of anterior head structure… Expand
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Highly Cited
1997
Highly Cited
1997
Renal cell carcinoma (RCC), a human kidney cancer from the proximal tubular epithelium, accounts for about 3% of adult… Expand
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Highly Cited
1992
Highly Cited
1992
Myotonic dystrophy (DM) is the most common inherited neuromuscular disease in adults, with a global incidence of 1 in 8000… Expand
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