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2q37.1

A chromosome band present on 2q
National Institutes of Health

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5 relations
ATG16L1 wt AlleleChromosomesEIF4E2 wt AlleleINPP5D 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.
2014
2014
Correlation of DNA methylation levels in blood and saliva DNA in young girls of the LEGACY Girls study
Many epidemiologic studies of environmental exposures and disease susceptibility measure DNA methylation in white blood cells… 
2013
2013
Genetic analysis of interferon induced thyroiditis (IIT): evidence for a key role for MHC and apoptosis related genes and pathways.
2012
2012
Dose dependent expression of HDAC4 causes variable expressivity in a novel inherited case of brachydactyly mental retardation syndrome
Histone deacetylase 4 (HDAC4) serves important roles in multiple human systems, including neurological, cardiac, and skeletal… 
2009
2009
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1
Posterior microphthalmia (PM) is a relatively rare autosomal recessive condition with normal anterior segment and small posterior… 
2006
2006
Oesophageal atresia with a terminal deletion of chromosome 2q37.1
We herein report the case of a newborn girl with oesophageal atresia associated with cardiac and gastrointestinal anomalies… 
2004
2004
Characterization of the human secreted phosphoprotein 24 gene (SPP2) and comparison of the protein sequence in nine species.
2001
2001
Holoprosencephaly associated with an apparent isolated 2q37.1-->2q37.3 deletion.
A female infant survived 5(1/2) hours after delivery at 33 weeks gestation. Autopsy showed a lobar variant of holoprosencephaly… 
2001
2001
Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1.
Gene duplication events are followed by divergence of initially identical gene copies, due to the subsequent accumulation of… 
1998
1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome
Here we report Wilms' tumor, gonadal dysgenesis and a bifid uterus in an 18‐month‐old female with a terminal deletion of the long… 
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