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9q22.32

A chromosome band present on 9q
National Institutes of Health

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Highly Cited
2015
Highly Cited
2015
Polycystic ovary syndrome (PCOS) is a common, highly heritable complex disorder of unknown aetiology characterized by… Expand
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Highly Cited
2012
Highly Cited
2012
Following a previous genome-wide association study (GWAS 1) including 744 cases and 895 controls, we analyzed genome-wide… Expand
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2010
2010
Cleft lip/palate comprises a large fraction of all human birth defects, and is notable for its significant lifelong morbidity and… Expand
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2009
2009
With the exception of the X chromosome, genomic deletions appear to be more prevalent than duplications. Because of a lack of… Expand
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Highly Cited
2008
Highly Cited
2008
IntroductionYounger women with breast carcinoma (BC) exhibits more aggressive pathologic features compared to older women; young… Expand
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Highly Cited
2006
Highly Cited
2006
Background: The best known hereditary colorectal cancer syndromes, familial adenomatous polyposis (FAP) and hereditary non… Expand
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2006
2006
To present the perinatal findings and the molecular cytogenetic analyses of a de novo interstitial deletion of 9q (9q22.3→q31.3… Expand
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Highly Cited
2005
Highly Cited
2005
Chromosomal instability, manifesting as copy number alterations (CNAs), is characteristic of pancreatic adenocarcinoma. We used… Expand
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2004
2004
Recently, we reported a whole genome scan on a sample of 630 Caucasian subjects from 53 human pedigrees. Several genomic regions… Expand
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Highly Cited
2002
Highly Cited
2002
The compact genome of the pufferfish, Fugu rubripes, has been proposed as a 'reference' genome to aid in annotating and analysing… Expand
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