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2p16

A chromosome band present on 2p
National Institutes of Health

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4 relations
Chromosome 2 Short ArmChromosomesEFEMP1 wt AlleleMSH6 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
A renal metanephric adenoma showing both a 2p16e24 deletion and BRAF V600E mutation: a synergistic role for a tumor suppressor gene on chromosome 2p and BRAF activation?
2006
2006
Microsatellite instability as an indicator of malignant progression in laryngeal premalignancy
Microsatellite instability (MSI) is considered a novel marker of genetic instability, and preliminary studies have shown that it… 
2006
2006
Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16.
We report three related and one unrelated child with an apparently novel neurodevelopmental disorder. The clinical course was… 
2004
2004
The replication error phenotype is associated with the development of distant metastases in hormonally treated patients with breast carcinoma
The positive replication error (RER+) phenotype defines a distinct subgroup of tumors with specific clinical, pathologic, and… 
2003
2003
A whole genome screen for association in Polish multiple sclerosis patients
2000
2000
Detection of two novel large deletions in SLC3A1 by semi‐quantitative fluorescent multiplex PCR
Cystinuria is an autosomal recessive aminoaciduria in which two clinical types have been described (type I and non‐type I… 
1999
1999
Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell lines
AbstractComparative genomic hybridization was used to identify chromosomal imbalances in eight cell lines and 12 blood samples… 
1999
1999
Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes.
The region of chromosome 2 encompassed by the polymorphic markers D2S378 (centromeric) and D2S391 (telomeric) spans an… 
1998
1998
Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes).
1998
1998
Evidence for a second genetic locus in Carney complex
Carney complex (MIM no. 160980) is an autosomal dominant condition of lentiginosis, cutaneous and cardiac myxomas and multiple… 
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