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19q13.1

A chromosome band present on 19q
National Institutes of Health

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Highly Cited
2008
Highly Cited
2008
Genome-wide association (GWA) studies have identified multiple loci at which common variants modestly influence the risk of… Expand
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Highly Cited
2003
Highly Cited
2003
Genome-wide copy number profiles were characterized in 41 primary bladder tumors using array-based comparative genomic… Expand
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Highly Cited
2000
Highly Cited
2000
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL; MIM 221770), also known as Nasu-Hakola… Expand
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Highly Cited
2000
Highly Cited
2000
Autosomal recessive Charcot-Marie-Tooth disease (CMT) type 4 (CMT4) is a complex group of demyelinating hereditary motor and… Expand
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Highly Cited
1999
Highly Cited
1999
Congenital nephrotic syndrome of the Finnish type (NPHS1) is an autosomal recessive disorder that is caused by mutations in the… Expand
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Highly Cited
1999
Highly Cited
1999
The Mixed Lineage Leukemia (MLL) gene is commonly involved in translocations in infantile leukemia and is amplified in some cases… Expand
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Highly Cited
1998
Highly Cited
1998
Febrile seizures affect approximately 3% of all children under six years of age and are by far the most common seizure disorder… Expand
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Highly Cited
1997
Highly Cited
1997
In our search for novel human galanin receptor (GALR) subtypes, human genomic DNA was PCR amplified using sets of degenerate… Expand
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Highly Cited
1996
Highly Cited
1996
In the human pancreatic cancer cell line PANC1, we detected several DNA fragments with abnormally intensified signals by… Expand
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Highly Cited
1991
Highly Cited
1991
We have detected transforming activity by a tumorigenicity assay using NIH3T3 cells transfected with DNA from a chronic… Expand
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