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7p22

A chromosome band present on 7p
National Institutes of Health

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12 relations
ACTB wt AlleleAIMP2 wt AlleleCARD11 wt AlleleChromosome 7 Short Arm

Papers overview

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2014
2014
SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot
SNX8: A Candidate Gene for 7p22 Cardiac Malformations Including Tetralogy of Fallot Rena J. Vanzo,* Megan M. Martin, Mallory R… 
2008
2008
Genetic alterations in a papillary glioneuronal tumor.
Papillary glioneuronal tumors (PGNTs) are rare lesions of the central nervous system, and no information exists on the genetic… 
2004
2004
Retention of heterozygosity at chromosome 7p22 and 11q13 in aldosterone-producing tumours of patients with familial hyperaldosteronism not remediable by glucocorticoids
Retention of heterozygosity at chromosome 7p22 and 11q13 in aldosterone-producing tumours of patients with familial… 
Highly Cited
2000
Highly Cited
2000
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes.
Retinal fascin is a newly identified photoreceptor-specific paralog of the actin-bundling protein fascin. Fascins crosslink f… 
1998
1998
Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13.
Among 23 squamous cell carcinomas (SCC) of the oral cavity which were screened for DNA copy number alterations (CNAs) using… 
Highly Cited
1994
Highly Cited
1994
cDNA cloning and expression of the human homolog of the sea urchin fascin and Drosophila singed genes which encodes an actin-bundling protein.
cDNA clones having extensive sequence identity with the sea urchin fascin and the Drosophila singed gene products were isolated… 
1993
1993
Cytogenetic characterization of Epstein-Barr virus-associated T-cell malignancies.
Highly Cited
1991
Highly Cited
1991
Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering.
cDNA clones encoding zinc finger structures were isolated by screening Molt4 and Jurkat cDNA libraries with zinc finger consensus… 
1985
1985
De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
In the present paper a malformed male newborn is presented with de novo 2q3 trisomy/distal 7p22 monosomy and typical clinical… 
1976
1976
Mental retardation, malformation syndrome and partial 7p monosomy [45, XX, tdic (7;15) (p21;pll)]
A mentally retarded and malformed girl is described. Her karyotype was 45, XX, tdic(7;15) (p21;p11), i.e. she was monosomic for… 
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