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8q22-q23

A chromosome band present on 8q
National Institutes of Health

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ChromosomesEIF3E wt Allele

Papers overview

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2020
2020
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23).
2017
2017
Síndrome de Cohen diagnosticado con hibridación genómica comparativa por microarreglos
El sindrome de Cohen (SC) es una enfermedad genetica rara, con herencia autosomica recesiva. Se origina por danos en el gen… 
2006
2006
Frequent 7q gains in flow cytometric multiploid/hypertetraploid breast carcinomas: a study of chromosome imbalances by comparative genomic hybridisation
Objective: To investigate underlying genetic events associated with complex DNA ploidy breast carcinomas. Methods: Screening for… 
2004
2004
Cohen syndrome in the Ohio Amish
We describe eight members from two large Amish kindreds who share a phenotype characterized by early‐onset pigmentary retinopathy… 
Highly Cited
2003
Highly Cited
2003
High‐resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays
Conventional cytogenetic and comparative genomic hybridization (CGH) studies have shown that osteosarcomas (OSs) are… 
2002
2002
Rearrangement involving chromosomes 1 and 8 in a retroperitoneal lipoma.
2001
2001
An integrated physical map of 8q22-q24: use in positional cloning and deletion analysis of Langer-Giedion syndrome.
We have developed an integrated map for a 35-cM area of human chromosome 8 surrounding the Langer-Giedion syndrome deletion… 
1997
1997
The chromosome location of the human homolog of the mouse mammary tumor-associated gene INT6 and its status in human breast carcinomas.
The INT6 gene is a common integration site for the mouse mammary tumor virus in mouse mammary tumors. We have determined that the… 
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