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11q14

A chromosome band present on 11q
National Institutes of Health

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Highly Cited
2014
Highly Cited
2014
BACKGROUND Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations… Expand
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Highly Cited
2004
Highly Cited
2004
In this study, we performed high-resolution array comparative genomic hybridization with an array of 4153 bacterial artificial… Expand
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Highly Cited
2000
Highly Cited
2000
Prepubertal periodontitis (PPP) is a rare and rapidly progressive disease of young children that results in destruction of the… Expand
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Highly Cited
1999
Highly Cited
1999
Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyperkeratosis and severe early… Expand
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Highly Cited
1997
Highly Cited
1997
Genetic hearing impairment affects around 1 in every 2,000 births1. The bulk (approximately 70%) of genetic deafness is non… Expand
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1997
1997
The genetic basis and molecular pathogenesis of chronic lymphocytic leukemia (CLL) and the molecular mechanisms responsible for… Expand
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Highly Cited
1996
Highly Cited
1996
The translocation t(10;11)(p13;q14) is a recurring chromosomal abnormality that has been observed in patients with acute… Expand
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Highly Cited
1996
Highly Cited
1996
Aberrations of the long arm of chromosome 11 are among the most common chromosome abnormalities in lymphoproliferative disorders… Expand
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1994
1994
We describe the cytogenetic findings in five mucoepidermoid carcinomas (MEC) of the major and minor salivary glands. Three of the… Expand
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1990
1990
Tuberous sclerosis (TSC) is a dominantly inherited disorder characterized by hamartomas and hamartias in one or more organs, most… Expand
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