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7q21

A chromosome band present on 7q
National Institutes of Health

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5 relations
Chromosome 7qChromosomesFZD1 wt AlleleGNAI1 wt Allele

Papers overview

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2008
2008
Molecular dissection of the chromosome band 7q21 amplicon in gastroesophageal junction adenocarcinomas identifies cyclin‐dependent kinase 6 at both genomic and protein expression levels
Amplification of chromosome band 7q21 has been frequently detected in various types of cancer including gastroesophageal junction… 
2007
2007
Bivariate Whole Genome Linkage Analysis for Femoral Neck Geometric Parameters and Total Body Lean Mass
A genome‐wide bivariate analysis was conducted for femoral neck GPs and TBLM in a large white sample. We found QTLs shared by GPs… 
2006
2006
A novel deletion mutation in CCM1 gene (krit1) is detected in a Chinese family with cerebral cavernous malformations.
2004
2004
Clinico-pathological significance of cell-type-specific loss of heterozygosity on chromosome 7q21: analysis of 318 microdissected thyroid lesions.
A careful pathological examination often reveals the presence of different lesions at various stages of tumor progression and… 
2003
2003
Myoclonus in a patient with a deletion of the epsilon-sarcoglycan locus on chromosome 7q21.
Autosomal dominant myoclonus-dystonia syndrome (MDS) is characterized by myoclonic and/or dystonic movements with onset as early… 
2001
2001
Comparative genomic hybridization analysis of nasopharygeal carcinoma: consistent patterns of genetic aberrations and clinicopathological correlations.
Highly Cited
1995
Highly Cited
1995
A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.
Ectrodactyly (split hand/split foot malformation, SHSF) is a human limb malformation characterized by absent central digital rays… 
1991
1991
Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3
A case of bilateral split hand and split foot malformation is reported in a boy with a complex rearrangement of chromosome 7… 
Review
1990
Review
1990
Chromosomal patterns in human benign uterine leiomyomas.
1990
1990
Localisation of the gene encoding the catalytic γ subunit of phosphorylase kinase to human chromosome bands 7p12-q21
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