6p25

A chromosome band present on 6p
National Institutes of Health

Papers overview

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2012
2012
Periventricular Heterotopia With White Matter Abnormalities Associated With 6p25 Deletion Elena Cellini, Vittoria Disciglio… (More)
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2006
2006
Chromosomal deletions at 6p25-p24 are rare findings in patients with developmental delay. There is limited information about the… (More)
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Review
2005
Review
2005
Deletion of distal 6p is associated with a distinctive clinical phenotype including Axenfeld-Rieger malformation, hearing loss… (More)
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Highly Cited
2005
Highly Cited
2005
Mantle cell lymphoma (MCL) is characterized by 11q13 chromosomal translocation and CCND1 overexpression, but additional genomic… (More)
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2002
2002
PURPOSE Mutations in the forkhead transcription factor gene FOXC1 on 6p25 cause a range of ocular developmental abnormalities… (More)
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2000
2000
Mutations in the forkhead-like 7 (FKHL7) gene have been recently shown to cause juvenile glaucoma and anterior segment anomalies… (More)
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Highly Cited
1999
Highly Cited
1999
Recent application of nonparametric-linkage analysis to reading disability has implicated a putative quantitative-trait locus… (More)
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Highly Cited
1998
Highly Cited
1998
A number of different eye disorders with the presence of early-onset glaucoma as a component of the phenotype have been mapped to… (More)
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Highly Cited
1998
Highly Cited
1998
Genetic linkage, genome mismatch scanning, and analysis of patients with alterations of chromosome 6 have indicated that a major… (More)
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1996
1996
Autosomal dominant iridogoniodysgenesis anomaly (IGDA) is characterized by iris hypoplasia and goniodysgenesis with frequent… (More)
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