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19q12

A chromosome band present on 19q
National Institutes of Health

Papers overview

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2011
2011
IntroductionThe 19q12 locus is amplified in a subgroup of oestrogen receptor (ER)-negative grade III breast cancers. This… Expand
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Highly Cited
2010
Highly Cited
2010
We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected… Expand
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Highly Cited
2009
Highly Cited
2009
PURPOSE A significant number of women with serous ovarian cancer are intrinsically refractory to platinum-based treatment. We… Expand
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Review
2009
Review
2009
The CYP2A6 gene spans a region of approximately 6 kb pairs consisting of 9 exons and has been mapped to the long arm of… Expand
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Highly Cited
2002
Highly Cited
2002
Hirschsprung disease (HSCR), the most common hereditary cause of intestinal obstruction, shows considerable variation and complex… Expand
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Highly Cited
1999
Highly Cited
1999
Cystinuria (MIM 220100) is a common recessive disorder of renal reabsorption of cystine and dibasic amino acids. Mutations in… Expand
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Highly Cited
1999
Highly Cited
1999
By means of comparative genomic hybridization (CGH), we screened 58 primary gastric cancers for changes in copy number of DNA… Expand
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1995
1995
A point mutation in the gene encoding the skeletal muscle calcium release channel (RYR1) has been proposed as the probable cause… Expand
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Highly Cited
1993
Highly Cited
1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) has been recently reported… Expand
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Highly Cited
1990
Highly Cited
1990
Malignant hyperthermia (MH) is an inherited human skeletal muscle disorder and is one of the main causes of death due to… Expand
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