HTC2 gene

Known as: CXINSq27.1, CGH, hypertrichosis 2 (generalized, congenital) 
Human HTC2 gene is located within Xq24-q27.1 and the size of this phenotypic locus is not reported. This gene region has no known protein product… (More)
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
Recent array-based studies have detected a wealth of copy number variations (CNVs) in patients with autism spectrum disorders… (More)
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Highly Cited
2011
Highly Cited
2011
BACKGROUND Several randomized controlled trials have not shown a benefit from preimplantation genetic screening (PGS) biopsy of… (More)
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Highly Cited
2010
Highly Cited
2010
Prader–Willi syndrome (PWS) is a neurobehavioral disorder manifested by infantile hypotonia and feeding difficulties in infancy… (More)
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Highly Cited
2008
Highly Cited
2008
To identify genomic abnormalities characteristic of pancreatic ductal adenocarcinoma (PDAC) in vivo, a panel of 27 microdissected… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Sonic hedgehog (SHH) plays an important role in defining the anterior-posterior axis in the developing limbs. A highly… (More)
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Highly Cited
2007
Highly Cited
2007
Prostate cancer is clinically heterogeneous, ranging from indolent to lethal disease. Expression profiling previously defined… (More)
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Highly Cited
2007
Highly Cited
2007
Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently… (More)
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Highly Cited
2006
Highly Cited
2006
Recently, the application of array-based comparative genomic hybridization (array CGH) has improved rates of detection of… (More)
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Highly Cited
2006
Highly Cited
2006
Genomic imbalances are a major cause of constitutional and acquired disorders. Therefore, aneuploidy screening has become the… (More)
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Highly Cited
2004
Highly Cited
2004
Maternally derived duplication of the imprinted region of chromosome 15q11-q14 leads to a complex neurobehavioral phenotype that… (More)
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