7q21

A chromosome band present on 7q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1979-2017
05101519792017

Papers overview

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Highly Cited
2010
Highly Cited
2010
Heterozygous mutations in p63 are associated with split hand/foot malformations (SHFM), orofacial clefting, and ectodermal… (More)
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2008
2008
Genomic imprinting is a developmentally important mechanism that involves both differential DNA methylation and allelic histone… (More)
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2007
2007
We report on a 42-year-old female patient with an interstitial 16 Mb deletion in 7q21.1-21.3 and a balanced reciprocal… (More)
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2003
2003
Autosomal dominant myoclonus-dystonia syndrome (MDS) is characterized by myoclonic and/or dystonic movements with onset as early… (More)
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2003
2003
Several independent genome scans have revealed excess allele sharing in an overlapping 40 cM region of 7q21-34 in autism. DLX6… (More)
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Highly Cited
2001
Highly Cited
2001
A novel paternally expressed imprinted gene, PEG10 (Paternally Expressed 10), was identified on human chromosome 7q21. PEG10 is… (More)
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1999
1999
We investigated copy number aberrations in 29 primary tumors and 12 cell lines of esophageal squamous cell carcinoma (ESC) using… (More)
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Highly Cited
1997
Highly Cited
1997
Krev-1/rap1A is an evolutionarily conserved Ras-family GTPase whose cellular function remains unclear, but which has been… (More)
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Highly Cited
1996
Highly Cited
1996
Exactly 100 years ago, in 1896, Pendred first described the association of congenital deafness with thyroid goitre (MIM#274600)1… (More)
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Highly Cited
1986
Highly Cited
1986
The met oncogene activated in vitro by treatment of a human osteogenic sarcoma (HOS) cell line with N-methyl-N… (More)
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