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19q13.1

A chromosome band present on 19q
National Institutes of Health

Papers overview

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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
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
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
1998
Highly Cited
1998
The available human prostate cancer cell lines that are metastatic in athymic nude mice all have complex, highly aneuploid… Expand
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
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
Highly Cited
1994
Highly Cited
1994
Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepresentation of genetic material… Expand
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