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3q29

A chromosome band present on 3q
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Pancreatic cancer is the fourth leading cause of cancer death in the developed world. Both inherited high-penetrance mutations in… Expand
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2013
2013
Some copy number variants (CNVs) are strongly implicated in both schizophrenia and autism spectrum disorders (ASDs). Childhood… Expand
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Highly Cited
2011
Highly Cited
2011
OBJECTIVE To evaluate previously reported associations of copy number variants (CNVs) with schizophrenia and to identify… Expand
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Highly Cited
2010
Highly Cited
2010
Schizophrenia (SZ) is a severe psychiatric illness that affects approximately 1% of the population and has a strong genetic… Expand
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Highly Cited
2009
Highly Cited
2009
Copy number variants (CNVs) contribute to human genetic and phenotypic diversity. However, the distribution of larger CNVs in the… Expand
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Highly Cited
2008
Highly Cited
2008
BackgroundInterstitial deletions of 3q29 have been recently described as a microdeletion syndrome mediated by nonallelic… Expand
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Highly Cited
2008
Highly Cited
2008
Microdeletion and microduplication genetic syndromes are known to be a significant cause of developmental delay and dysmorphology… Expand
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Highly Cited
2005
Highly Cited
2005
We report the identification of six patients with 3q29 microdeletion syndrome. The clinical phenotype is variable despite an… Expand
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1996
1996
Abstract Dominant optic atrophy, type Kjer, is an autosomal dominant eye disease that is characterized by progressive optic… Expand
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Highly Cited
1995
Highly Cited
1995
We now report a mutation in the nuclear–encoded flavoprotein (Fp) subunit gene of the succinate dehydrogenase (SDH) in two… Expand
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