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2p25.3

A chromosome band present on 2p
National Institutes of Health

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Chromosome 2 Short ArmChromosomes

Papers overview

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2020
2020
Mid‐trimester fetal facial dysmorphology associated with 2p25.3 microdeletion
We describe unusual mid‐trimester sonography of subtle fetal facial dysmorphic features including; flattened nasofrontal angle… 
2014
2014
[Genetic diagnosis and analysis of related genes for a pedigree with 2p25 and 12p13 cryptic rearrangements].
OBJECTIVE To analyze chromosome aberration in a child with mental retardation and abnormalities and its parents. METHODS… 
2013
2013
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
2011
2011
Common genomic aberrations in basaloid squamous cell carcinoma and carcinosarcoma of the esophagus detected by CGH and array CGH.
Basaloid squamous cell carcinoma (BSCC) and carcinosarcoma of the esophagus are rare entities, making up fewer than 2% of… 
2007
2007
Genome-wide examination of chromosomal aberrations in neuroblastoma SH-SY5Y cells by array-based comparative genomic hybridization.
2007
2007
Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23‐pter
Inverted duplications with terminal deletions have been reported in an increasing number of chromosomes and are probably more… 
2006
2006
Triallelic patterns in STR loci used for paternity analysis: evidence for a duplication in chromosome 2 containing the TPOX STR locus.
1999
1999
An unbalanced half‐cryptic translocation involving the 6q subtelomeric region and 2p25.3 in a child with mental retardation: uses and limitations of fluorescence insitu hybridization
We report on a 5‐year‐old boy with minor anomalies, growth retardation, and developmental delay carrying an extra chromatin… 
1994
1994
Assignment of a human melanoma associated gene MG50 (D2S448) to chromosome 2p25.3 by fluorescence in situ hybridization.
To identify the chromosomal locus encoding this gene, 1 {mu}g of a human genomic clone (G23MG5), which is 17.25-kb and contains… 
1982
1982
Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange.
A 5-year-old male with mild mental retardation showed a chromosomal rearrangement involving duplication of part of 2q (2q33.3… 
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