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5q11.2

A chromosome band present on 5q
National Institutes of Health

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5 relations
ChromosomesESM1 wt AlleleMAP3K1 wt AllelePELO wt Allele

Papers overview

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2015
2015
High-resolution 400K oligonucleotide array comparative genomic hybridization analysis of neurofibromatosis type 1-associated cutaneous neurofibromas.
2012
2012
Rat Mcs1b is concordant to the genome-wide association-identified breast cancer risk locus at human 5q11.2 and MIER3 is a candidate cancer susceptibility gene.
Low-penetrance alleles associated with breast cancer risk have been identified in population-based studies. Most risk loci… 
Review
2012
Review
2012
Drug treatment for spinal muscular atrophy types II and III.
BACKGROUND Spinal muscular atrophy (SMA) is caused by degeneration of anterior horn cells, which leads to progressive muscle… 
2012
2012
Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array.
2010
2010
5q11.2 deletion in a patient with tracheal agenesis
Tracheal agenesis (TA) is a rare congenital anomaly of the respiratory tract. Many patients have associated anomalies, suggesting… 
2003
2003
Comprehensive genome-wide comparison of DNA and RNA level scan using microarray technology for identification of candidate cancer-related genes in the HL-60 cell line.
1992
1992
A genetic linkage study of schizophrenia to chromosome 5 markers in a Northern Italian population
1990
1990
Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia.
We report on 2 relatives with a segmental duplication of 5q11.2----13.3. The phenotype is surprisingly limited for the degree of… 
1989
1989
Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia.
1989
1989
Duplication of 5q11.2----q13.1 from a familial (5;20) balanced insertion.
A 2-year-old boy with gross motor delay and few minor anomalies has a pure duplication of a small segment of chromosome 5q11.2… 
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