14q12

A chromosome band present on 14q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1975-2018
024619752018

Papers overview

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2013
2013
Rett syndrome is a clinically defined neurodevelopmental disorder almost exclusively affecting females. Usually sporadic, Rett… (More)
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2012
2012
The Forkhead box G1 (FOXG1) gene has been implicated in severe Rett-like phenotypes. It encodes the Forkhead box protein G1, a… (More)
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2011
2011
Genome-wide high-resolution array analysis is rapidly becoming a reliable method of diagnostic investigation in individuals with… (More)
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2009
2009
Only two patients with 14q12 deletion have been reported to date. Here, we describe an additional patient with a similar deletion… (More)
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2009
2009
Microdeletions at 14q12 that include FOXG1, or loss of function mutations in FOXG1, are associated with the congenital variant of… (More)
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Highly Cited
2009
Highly Cited
2009
PURPOSE To characterize the molecular genetic profiles of grade 3 invasive ductal carcinomas of no special type using high… (More)
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2008
2008
Previous genome-wide linkage studies applied the affected sib-pair design; one investigated extended pedigrees of a genetic… (More)
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2005
Highly Cited
2005
Atrial septal defect is one of the most common forms of congenital heart malformation. We identified a new locus linked with… (More)
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1996
1996
We report a novel locus responsible for postlingual progressive sensorineural hearing loss (designated DFNA9) that maps to… (More)
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1985
1985
A cDNA clone encoding the alpha chain of the human T cell receptor was used in connection with somatic cell human-rodent hybrids… (More)
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