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8q22-q23

A chromosome band present on 8q
National Institutes of Health

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2 relations
ChromosomesEIF3E wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23).
OBJECTIVE We present prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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2002
2002
Rearrangement involving chromosomes 1 and 8 in a retroperitoneal lipoma.
Superficial lipomas are very common benign adipose tissue tumors. In contrast, deep-seated lipomas such as retroperitoneal… Expand
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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… Expand
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2000
2000
Genetic aberrations detected by comparative genomic hybridization predict outcome in patients with endometrioid carcinoma.
Endometrial cancer progression is determined by a complex pattern of multiple genetic aberrations, but how these aberrations… Expand
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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… Expand
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